Canonical Allele Identifier: CA399304962
Gene: TCAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665904G>T , CM000679.2:g.39665904G>T GRCh38
NC_000017.10:g.37822157G>T , CM000679.1:g.37822157G>T GRCh37
NC_000017.9:g.35075683G>T NCBI36
NG_008892.1:g.5559G>T , LRG_210:g.5559G>T
NG_042278.1:g.2924G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.3:c.299G>T MANE Select ENSP00000312624.2:p.Gly100Val
ENST00000309889.2:c.299G>T ENSP00000312624.2:p.Gly100Val
ENST00000578283.1:c.227G>T ENSP00000462787.1:p.Gly76Val
NM_003673.3:c.299G>T , LRG_210t1:c.299G>T NP_003664.1:p.Gly100Val
NM_003673.4:c.299G>T MANE Select NP_003664.1:p.Gly100Val