Canonical Allele Identifier: CA399302863
Gene: TCAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665415A>T , CM000679.2:g.39665415A>T GRCh38
NC_000017.10:g.37821668A>T , CM000679.1:g.37821668A>T GRCh37
NC_000017.9:g.35075194A>T NCBI36
NG_008892.1:g.5070A>T , LRG_210:g.5070A>T
NG_042278.1:g.2435A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.3:c.56A>T MANE Select ENSP00000312624.2:p.Glu19Val
ENST00000309889.2:c.56A>T ENSP00000312624.2:p.Glu19Val
ENST00000578283.1:c.56A>T ENSP00000462787.1:p.Glu19Val
NM_003673.3:c.56A>T , LRG_210t1:c.56A>T NP_003664.1:p.Glu19Val
NM_003673.4:c.56A>T MANE Select NP_003664.1:p.Glu19Val