Canonical Allele Identifier: CA399305057
Gene: TCAP HGNC NCBI

Linked Data

ClinVar Variation Id: 1297610
ClinVar RCV Id: RCV001723378
dbSNP Id: rs2145073848

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665915G>A , CM000679.2:g.39665915G>A GRCh38
NC_000017.10:g.37822168G>A , CM000679.1:g.37822168G>A GRCh37
NC_000017.9:g.35075694G>A NCBI36
NG_008892.1:g.5570G>A , LRG_210:g.5570G>A
NG_042278.1:g.2935G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.3:c.310G>A MANE Select ENSP00000312624.2:p.Glu104Lys
ENST00000309889.2:c.310G>A ENSP00000312624.2:p.Glu104Lys
ENST00000578283.1:c.238G>A ENSP00000462787.1:p.Glu80Lys
NM_003673.3:c.310G>A , LRG_210t1:c.310G>A NP_003664.1:p.Glu104Lys
NM_003673.4:c.310G>A MANE Select NP_003664.1:p.Glu104Lys