Canonical Allele Identifier: CA399305328
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs2145074098

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665966A>G , CM000679.2:g.39665966A>G GRCh38
NC_000017.10:g.37822219A>G , CM000679.1:g.37822219A>G GRCh37
NC_000017.9:g.35075745A>G NCBI36
NG_008892.1:g.5621A>G , LRG_210:g.5621A>G
NG_042278.1:g.2986A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.3:c.361A>G MANE Select ENSP00000312624.2:p.Thr121Ala
ENST00000309889.2:c.361A>G ENSP00000312624.2:p.Thr121Ala
ENST00000578283.1:c.289A>G ENSP00000462787.1:p.Thr97Ala
NM_003673.3:c.361A>G , LRG_210t1:c.361A>G NP_003664.1:p.Thr121Ala
NM_003673.4:c.361A>G MANE Select NP_003664.1:p.Thr121Ala