Linked Data
dbSNP Id:
rs953856612
gnomAD v2:
12-54677761-C-G
gnomAD v4:
12-54283977-C-G
MyVariant Identifiers:
chr12:g.54677761_54677763delinsGTA (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.54283977C>G , CM000674.2:g.54283977C>G | GRCh38 |
| NC_000012.11:g.54677761C>G , CM000674.1:g.54677761C>G | GRCh37 |
| NC_000012.10:g.52964028C>G | NCBI36 |
| NG_033830.1:g.8274C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000340913.11:c.1063+10C>G MANE Select | ENSP00000341826.7:n.1063+10C>G | |
| ENST00000550482.2:c.907+10C>G | ENSP00000446486.2:n.907+10C>G | |
| ENST00000676572.1:c.289+10C>G | ||
| ENST00000676725.1:n.1237+10C>G | ||
| ENST00000676794.1:c.82+10C>G | ENSP00000504819.1:n.82+10C>G | |
| ENST00000676886.1:c.85-281C>G | ||
| ENST00000677191.1:c.403+10C>G | ||
| ENST00000677210.1:c.1063+10C>G | ENSP00000503610.1:n.1063+10C>G | |
| ENST00000677220.1:c.132+2475C>G | ENSP00000502987.1:n.132+2475C>G | |
| ENST00000677249.1:c.904+10C>G | ENSP00000503649.1:n.904+10C>G | |
| ENST00000677375.1:c.907+10C>G | ENSP00000503651.1:n.907+10C>G | |
| ENST00000677385.1:c.*1259C>G | ENSP00000502985.1:n.*1259C>G | |
| ENST00000677778.1:c.75+1103C>G | ||
| ENST00000677840.1:c.156+10C>G | ||
| ENST00000678077.1:c.772+10C>G | ENSP00000504814.1:n.772+10C>G | |
| ENST00000678212.1:c.251+10C>G | ||
| ENST00000678365.1:n.49-2685C>G | ||
| ENST00000678412.1:c.157-281C>G | ||
| ENST00000678418.1:n.1259+10C>G | ||
| ENST00000678448.1:c.255+10C>G | ENSP00000503619.1:n.255+10C>G | |
| ENST00000678456.1:c.76-281C>G | ||
| ENST00000678970.1:c.232+10C>G | ||
| ENST00000679026.1:c.156+10C>G | ||
| ENST00000679079.1:c.157-572C>G | ||
| ENST00000679228.1:n.1258+10C>G | ||
| ENST00000679273.1:c.243+10C>G | ENSP00000504626.1:n.243+10C>G | |
| ENST00000679344.1:c.264+10C>G | ||
| ENST00000330752.12:c.868+10C>G | ENSP00000333504.8:n.868+10C>G | |
| ENST00000340913.10:c.1063+10C>G | ENSP00000341826.6:n.1063+10C>G | |
| ENST00000546500.5:c.907+10C>G | ENSP00000448617.1:n.907+10C>G | |
| ENST00000547276.5:c.748+10C>G | ENSP00000447260.1:n.748+10C>G | |
| ENST00000547566.5:c.907+10C>G | ENSP00000449913.1:n.907+10C>G | |
| ENST00000550482.1:c.520+10C>G | ENSP00000446486.1:n.520+10C>G | |
| ENST00000551679.1:n.245+10C>G | ||
| NM_002136.2:c.907+10C>G | NP_002127.1:n.907+10C>G | |
| NM_031157.2:c.1063+10C>G | NP_112420.1:n.1063+10C>G | |
| XM_005268826.1:c.1063+10C>G | XP_005268883.1:n.1063+10C>G | |
| XR_245923.1:n.1175+10C>G | ||
| XR_245924.1:n.1019+10C>G | ||
| NM_002136.3:c.907+10C>G | NP_002127.1:n.907+10C>G | |
| NM_031157.3:c.1063+10C>G | NP_112420.1:n.1063+10C>G | |
| NR_135167.1:n.1025+10C>G | ||
| XM_005268826.2:c.1063+10C>G | XP_005268883.1:n.1063+10C>G | |
| XR_245923.2:n.1135+10C>G | ||
| NM_002136.4:c.907+10C>G | NP_002127.1:n.907+10C>G | |
| NM_031157.4:c.1063+10C>G MANE Select | NP_112420.1:n.1063+10C>G | |
| NR_135167.2:n.989+10C>G |