UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Linked Data
ClinVar Variation Id:
1326734
ClinVar RCV Id:
RCV001786914
dbSNP Id:
rs2134456336
gnomAD v4:
9-95107237-C-T
MyVariant Identifiers:
chr9:g.97869519C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.95107237C>T , CM000671.2:g.95107237C>T | GRCh38 |
| NC_000009.11:g.97869519C>T , CM000671.1:g.97869519C>T | GRCh37 |
| NC_000009.10:g.96909340C>T | NCBI36 |
| NG_011707.1:g.215473G>A , LRG_497:g.215473G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000710812.1:n.410+26457C>T (AOPEP) | ||
| ENST00000696260.1:n.2177G>A (FANCC) | ||
| ENST00000289081.8:c.1362G>A (FANCC) MANE Select | ENSP00000289081.3:p.Leu454= | |
| ENST00000375305.6:c.1362G>A (FANCC) | ENSP00000364454.1:p.Leu454= | |
| ENST00000649334.1:c.1507G>A (FANCC) | ENSP00000497735.1:n.1507G>A | |
| ENST00000289081.7:c.1362G>A (FANCC) | ENSP00000289081.3:p.Leu454= | |
| ENST00000375305.5:c.1362G>A (FANCC) | ENSP00000364454.1:p.Leu454= | |
| ENST00000464627.5:n.689G>A (FANCC) | ||
| NM_000136.2:c.1362G>A , LRG_497t1:c.1362G>A (FANCC) | NP_000127.2:p.Leu454= | |
| NM_001243743.1:c.1362G>A (FANCC) | NP_001230672.1:p.Leu454= | |
| XM_005251802.2:c.681G>A (FANCC) | XP_005251859.1:p.Leu227= | |
| XM_006717001.1:c.1197G>A (FANCC) | XP_006717064.1:p.Leu399= | |
| XM_011518365.1:c.1362G>A (FANCC) | XP_011516667.1:p.Leu454= | |
| XM_011518367.1:c.906G>A (FANCC) | XP_011516669.1:p.Leu302= | |
| XM_011519121.1:c.2319+26457C>T (AOPEP) | XP_011517423.1:n.2319+26457C>T | |
| XM_005251802.3:c.681G>A (FANCC) | XP_005251859.1:p.Leu227= | |
| XM_006717001.3:c.1197G>A (FANCC) | XP_006717064.1:p.Leu399= | |
| XM_011518365.3:c.1362G>A (FANCC) | XP_011516667.1:p.Leu454= | |
| XM_011518367.2:c.906G>A (FANCC) | XP_011516669.1:p.Leu302= | |
| XM_011519121.3:c.2319+26457C>T (AOPEP) | XP_011517423.1:n.2319+26457C>T | |
| XM_017014452.2:c.906G>A (FANCC) | XP_016869941.1:p.Leu302= | |
| XM_017014453.1:c.906G>A (FANCC) | XP_016869942.1:p.Leu302= | |
| XM_017014454.1:c.741G>A (FANCC) | XP_016869943.1:p.Leu247= | |
| XM_024447451.1:c.1362G>A (FANCC) | XP_024303219.1:p.Leu454= | |
| XR_001746847.1:n.655C>T | ||
| NM_000136.3:c.1362G>A (FANCC) MANE Select | NP_000127.2:p.Leu454= | |
| NM_001243743.2:c.1362G>A (FANCC) | NP_001230672.1:p.Leu454= |