Canonical Allele Identifier: CA399305859
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs2145074580

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39666035G>T , CM000679.2:g.39666035G>T GRCh38
NC_000017.10:g.37822288G>T , CM000679.1:g.37822288G>T GRCh37
NC_000017.9:g.35075814G>T NCBI36
NG_008892.1:g.5690G>T , LRG_210:g.5690G>T
NG_042278.1:g.3055G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.3:c.430G>T MANE Select ENSP00000312624.2:p.Val144Leu
ENST00000309889.2:c.430G>T ENSP00000312624.2:p.Val144Leu
ENST00000578283.1:c.358G>T ENSP00000462787.1:p.Val120Leu
NM_003673.3:c.430G>T , LRG_210t1:c.430G>T NP_003664.1:p.Val144Leu
NM_003673.4:c.430G>T MANE Select NP_003664.1:p.Val144Leu