Canonical Allele Identifier: CA399305818
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs45509691

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39666026C>A , CM000679.2:g.39666026C>A GRCh38
NC_000017.10:g.37822279C>A , CM000679.1:g.37822279C>A GRCh37
NC_000017.9:g.35075805C>A NCBI36
NG_008892.1:g.5681C>A , LRG_210:g.5681C>A
NG_042278.1:g.3046C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.3:c.421C>A MANE Select ENSP00000312624.2:p.Pro141Thr
ENST00000309889.2:c.421C>A ENSP00000312624.2:p.Pro141Thr
ENST00000578283.1:c.349C>A ENSP00000462787.1:p.Pro117Thr
NM_003673.3:c.421C>A , LRG_210t1:c.421C>A NP_003664.1:p.Pro141Thr
NM_003673.4:c.421C>A MANE Select NP_003664.1:p.Pro141Thr