Canonical Allele Identifier: CA499670373
Gene: TCAP HGNC NCBI

Linked Data

ClinVar Variation Id: 2940721
ClinVar RCV Id: RCV003800031
MyVariant Identifiers: chr17:g.37821705C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665452C>A , CM000679.2:g.39665452C>A GRCh38
NC_000017.10:g.37821705C>A , CM000679.1:g.37821705C>A GRCh37
NC_000017.9:g.35075231C>A NCBI36
NG_008892.1:g.5107C>A , LRG_210:g.5107C>A
NG_042278.1:g.2472C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.3:c.93C>A MANE Select ENSP00000312624.2:p.Ser31=
ENST00000309889.2:c.93C>A ENSP00000312624.2:p.Ser31=
ENST00000578283.1:c.93C>A ENSP00000462787.1:p.Ser31=
NM_003673.3:c.93C>A , LRG_210t1:c.93C>A NP_003664.1:p.Ser31=
NM_003673.4:c.93C>A MANE Select NP_003664.1:p.Ser31=
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