Canonical Allele Identifier: CA399305466
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs2145074243

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665990G>T , CM000679.2:g.39665990G>T GRCh38
NC_000017.10:g.37822243G>T , CM000679.1:g.37822243G>T GRCh37
NC_000017.9:g.35075769G>T NCBI36
NG_008892.1:g.5645G>T , LRG_210:g.5645G>T
NG_042278.1:g.3010G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.3:c.385G>T MANE Select ENSP00000312624.2:p.Asp129Tyr
ENST00000309889.2:c.385G>T ENSP00000312624.2:p.Asp129Tyr
ENST00000578283.1:c.313G>T ENSP00000462787.1:p.Asp105Tyr
NM_003673.3:c.385G>T , LRG_210t1:c.385G>T NP_003664.1:p.Asp129Tyr
NM_003673.4:c.385G>T MANE Select NP_003664.1:p.Asp129Tyr