Linked Data
gnomAD v2:
20-31023720-GTA-G
gnomAD v4:
20-32435917-GTA-G
MyVariant Identifiers:
chr20:g.31023721_31023722del (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.32435919_32435920del , CM000682.2:g.32435919_32435920del | GRCh38 |
| NC_000020.10:g.31023722_31023723del , CM000682.1:g.31023722_31023723del | GRCh37 |
| NC_000020.9:g.30487383_30487384del | NCBI36 |
| NG_027868.1:g.82576_82577del , LRG_630:g.82576_82577del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375687.10:c.3207_3208del MANE Select | ENSP00000364839.4:p.Ala1071GlyfsTer15 | |
| ENST00000646985.1:c.3024_3025del | ENSP00000495053.1:p.Ala1010GlyfsTer15 | |
| ENST00000647223.1:n.5560_5561del | ||
| ENST00000651418.1:c.1869+1338_1869+1339del | ENSP00000499150.1:n.1869+1338_1869+1339del | |
| ENST00000306058.9:c.3192_3193del | ENSP00000305119.5:p.Ala1066GlyfsTer15 | |
| ENST00000375687.8:c.3207_3208del | ENSP00000364839.4:p.Ala1071GlyfsTer15 | |
| ENST00000613218.4:c.3207_3208del | ENSP00000480487.1:p.Ala1071GlyfsTer15 | |
| ENST00000620121.4:c.3207_3208del | ENSP00000481978.1:p.Ala1071GlyfsTer15 | |
| NM_015338.5:c.3207_3208del , LRG_630t1:c.3207_3208del | NP_056153.2:p.Ala1071GlyfsTer15 | |
| XM_006723727.2:c.3204_3205del | XP_006723790.1:p.Ala1070GlyfsTer15 | |
| XM_006723728.2:c.3177_3178del | XP_006723791.1:p.Ala1061GlyfsTer15 | |
| XM_006723730.2:c.3123_3124del | XP_006723793.1:p.Ala1043GlyfsTer15 | |
| XM_006723732.2:c.3024_3025del | XP_006723795.1:p.Ala1010GlyfsTer15 | |
| XM_006723733.1:c.2523_2524del | XP_006723796.1:p.Ala843GlyfsTer15 | |
| XM_011528647.1:c.3471_3472del | XP_011526949.1:p.Ala1159GlyfsTer15 | |
| XM_011528648.1:c.3468_3469del | XP_011526950.1:p.Ala1158GlyfsTer15 | |
| XM_011528649.1:c.3387_3388del | XP_011526951.1:p.Ala1131GlyfsTer15 | |
| XM_011528650.1:c.3318_3319del | XP_011526952.1:p.Ala1108GlyfsTer15 | |
| XM_011528651.1:c.3186_3187del | XP_011526953.1:p.Ala1064GlyfsTer15 | |
| XM_011528652.1:c.3123_3124del | XP_011526954.1:p.Ala1043GlyfsTer15 | |
| NM_001363734.1:c.3024_3025del | NP_001350663.1:p.Ala1010GlyfsTer15 | |
| XM_006723727.3:c.3204_3205del | XP_006723790.1:p.Ala1070GlyfsTer15 | |
| XM_006723728.3:c.3177_3178del | XP_006723791.1:p.Ala1061GlyfsTer15 | |
| XM_006723730.4:c.3123_3124del | XP_006723793.1:p.Ala1043GlyfsTer15 | |
| XM_011528648.3:c.3468_3469del | XP_011526950.1:p.Ala1158GlyfsTer15 | |
| XM_011528652.2:c.3123_3124del | XP_011526954.1:p.Ala1043GlyfsTer15 | |
| XM_017027704.1:c.3123_3124del | XP_016883193.1:p.Ala1043GlyfsTer15 | |
| XM_017027705.1:c.3123_3124del | XP_016883194.1:p.Ala1043GlyfsTer15 | |
| XM_017027706.1:c.3054_3055del | XP_016883195.1:p.Ala1020GlyfsTer15 | |
| NM_015338.6:c.3207_3208del MANE Select | NP_056153.2:p.Ala1071GlyfsTer15 |