Linked Data
ClinVar Variation Id:
2152899
ClinVar RCV Id:
RCV003077335
dbSNP Id:
rs763730339
ExAC:
4:128842878 A / G
gnomAD v2:
4-128842878-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.127921723A>G , CM000666.2:g.127921723A>G | GRCh38 |
| NC_000004.11:g.128842878A>G , CM000666.1:g.128842878A>G | GRCh37 |
| NC_000004.10:g.129062328A>G | NCBI36 |
| NG_008657.1:g.49262T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296468.8:c.1151T>C | ENSP00000296468.3:p.Ile384Thr | |
| ENST00000509826.2:c.*472T>C | ENSP00000421176.2:n.*472T>C | |
| ENST00000513559.6:c.869T>C | ENSP00000425000.2:p.Ile290Thr | |
| ENST00000515130.6:c.*36T>C | ENSP00000493056.1:n.*36T>C | |
| ENST00000641025.1:c.*36T>C | ENSP00000493346.1:n.*36T>C | |
| ENST00000641092.1:c.*36T>C | ENSP00000493392.1:n.*36T>C | |
| ENST00000641133.1:c.*465T>C | ENSP00000493192.1:n.*465T>C | |
| ENST00000641146.1:n.1017T>C | ||
| ENST00000641147.1:c.701T>C | ENSP00000493133.1:p.Ile234Thr | |
| ENST00000641178.1:c.1016T>C | ENSP00000492989.1:p.Ile339Thr | |
| ENST00000641186.1:c.1037T>C | ENSP00000493347.1:p.Ile346Thr | |
| ENST00000641228.1:c.*36T>C | ENSP00000493194.1:n.*36T>C | |
| ENST00000641332.1:c.*212T>C | ENSP00000493397.1:n.*212T>C | |
| ENST00000641340.1:c.*280T>C | ENSP00000493191.1:n.*280T>C | |
| ENST00000641388.1:n.398T>C | ||
| ENST00000641393.1:c.701T>C | ENSP00000493197.1:p.Ile234Thr | |
| ENST00000641397.1:c.*36T>C | ENSP00000493406.1:n.*36T>C | |
| ENST00000641413.1:c.76T>C | ||
| ENST00000641434.1:c.1151T>C | ENSP00000493279.1:p.Ile384Thr | |
| ENST00000641464.1:c.*384T>C | ENSP00000493438.1:n.*384T>C | |
| ENST00000641482.1:c.*36T>C | ENSP00000493277.1:n.*36T>C | |
| ENST00000641508.1:c.*384T>C | ENSP00000493209.1:n.*384T>C | |
| ENST00000641509.1:c.836T>C | ENSP00000493459.1:p.Ile279Thr | |
| ENST00000641590.1:c.*36T>C | ENSP00000493132.1:n.*36T>C | |
| ENST00000641658.1:c.*316T>C | ENSP00000492987.1:n.*316T>C | |
| ENST00000641686.2:c.1151T>C MANE Select | ENSP00000493218.2:p.Ile384Thr | |
| ENST00000641690.1:c.950T>C | ENSP00000492966.1:p.Ile317Thr | |
| ENST00000641742.1:c.*316T>C | ENSP00000493315.1:n.*316T>C | |
| ENST00000641748.1:c.1151T>C | ENSP00000493330.1:p.Ile384Thr | |
| ENST00000641753.1:c.978T>C | ||
| ENST00000641774.1:c.*403T>C | ENSP00000492960.1:n.*403T>C | |
| ENST00000641830.1:c.383T>C | ||
| ENST00000641843.1:c.*212T>C | ENSP00000493174.1:n.*212T>C | |
| ENST00000641869.1:c.352T>C | ||
| ENST00000641870.1:c.*212T>C | ENSP00000493044.1:n.*212T>C | |
| ENST00000641882.1:c.*316T>C | ENSP00000493301.1:n.*316T>C | |
| ENST00000641928.1:c.*280T>C | ENSP00000493418.1:n.*280T>C | |
| ENST00000641949.1:c.554-887T>C | ENSP00000492891.1:n.554-887T>C | |
| ENST00000642012.1:n.1015T>C | ||
| ENST00000642034.1:c.*36T>C | ENSP00000493285.1:n.*36T>C | |
| ENST00000642042.1:c.1151T>C | ENSP00000493260.1:p.Ile384Thr | |
| ENST00000642078.1:c.*212T>C | ENSP00000492885.1:n.*212T>C | |
| ENST00000296468.7:c.1151T>C | ENSP00000296468.3:p.Ile384Thr | |
| ENST00000504126.1:n.179T>C | ||
| ENST00000513559.5:c.1016T>C | ENSP00000425000.1:p.Ile339Thr | |
| ENST00000515130.5:n.1493T>C | ||
| NM_152778.2:c.1151T>C | NP_689991.1:p.Ile384Thr | |
| XM_005262893.1:c.1151T>C | XP_005262950.1:p.Ile384Thr | |
| XM_005262896.1:c.1004T>C | XP_005262953.1:p.Ile335Thr | |
| XM_005262897.1:c.950T>C | XP_005262954.1:p.Ile317Thr | |
| XM_005262898.2:c.*36T>C | XP_005262955.1:n.*36T>C | |
| XM_011531830.1:c.1037T>C | XP_011530132.1:p.Ile346Thr | |
| XM_011531831.1:c.836T>C | XP_011530133.1:p.Ile279Thr | |
| XM_011531832.1:c.*36T>C | XP_011530134.1:n.*36T>C | |
| XR_938717.1:n.1228T>C | ||
| NM_001363520.1:c.950T>C | NP_001350449.1:p.Ile317Thr | |
| NM_001363521.1:c.836T>C | NP_001350450.1:p.Ile279Thr | |
| XM_005262898.3:c.*36T>C | XP_005262955.1:n.*36T>C | |
| XM_017007989.1:c.*36T>C | XP_016863478.1:n.*36T>C | |
| XM_024453981.1:c.1016T>C | XP_024309749.1:p.Ile339Thr | |
| XM_024453982.1:c.902T>C | XP_024309750.1:p.Ile301Thr | |
| XM_024453983.1:c.701T>C | XP_024309751.1:p.Ile234Thr | |
| XR_001741194.1:n.1124T>C | ||
| XR_001741195.1:n.1010T>C | ||
| XR_001741196.1:n.923T>C | ||
| XR_001741197.1:n.1083T>C | ||
| XR_001741198.2:n.979T>C | ||
| XR_001741199.1:n.979T>C | ||
| XR_938717.2:n.1228T>C | ||
| NM_001363520.2:c.950T>C | NP_001350449.1:p.Ile317Thr | |
| NM_001363521.2:c.836T>C | NP_001350450.1:p.Ile279Thr | |
| NM_001371590.1:c.1016T>C | NP_001358519.1:p.Ile339Thr | |
| NM_001371591.1:c.1151T>C | NP_001358520.1:p.Ile384Thr | |
| NM_001371592.1:c.1157T>C | NP_001358521.1:p.Ile386Thr | |
| NM_001371593.1:c.1037T>C | NP_001358522.1:p.Ile346Thr | |
| NM_001371594.1:c.1004T>C | NP_001358523.1:p.Ile335Thr | |
| NM_001371595.1:c.869T>C | NP_001358524.1:p.Ile290Thr | |
| NM_001371596.2:c.1151T>C MANE Select | NP_001358525.1:p.Ile384Thr | |
| NM_152778.3:c.1151T>C | NP_689991.1:p.Ile384Thr | |
| NM_152778.4:c.1151T>C | NP_689991.1:p.Ile384Thr |