Canonical Allele Identifier: CA163427
Gene: TCAP HGNC NCBI

Linked Data

ClinVar Variation Id: 140582
ClinVar RCV Id: RCV000128799
dbSNP Id: rs45495192

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665391C>A , CM000679.2:g.39665391C>A GRCh38
NC_000017.10:g.37821644C>A , CM000679.1:g.37821644C>A GRCh37
NC_000017.9:g.35075170C>A NCBI36
NG_008892.1:g.5046C>A , LRG_210:g.5046C>A
NG_042278.1:g.2411C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.3:c.32C>A MANE Select ENSP00000312624.2:p.Ser11Ter
ENST00000309889.2:c.32C>A ENSP00000312624.2:p.Ser11Ter
ENST00000578283.1:c.32C>A ENSP00000462787.1:p.Ser11Ter
NM_003673.3:c.32C>A , LRG_210t1:c.32C>A NP_003664.1:p.Ser11Ter
NM_003673.4:c.32C>A MANE Select NP_003664.1:p.Ser11Ter