Canonical Allele Identifier: CA399304485
Gene: TCAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665850A>C , CM000679.2:g.39665850A>C GRCh38
NC_000017.10:g.37822103A>C , CM000679.1:g.37822103A>C GRCh37
NC_000017.9:g.35075629A>C NCBI36
NG_008892.1:g.5505A>C , LRG_210:g.5505A>C
NG_042278.1:g.2870A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.3:c.245A>C MANE Select ENSP00000312624.2:p.Gln82Pro
ENST00000309889.2:c.245A>C ENSP00000312624.2:p.Gln82Pro
ENST00000578283.1:c.175-2A>C ENSP00000462787.1:n.175-2A>C
NM_003673.3:c.245A>C , LRG_210t1:c.245A>C NP_003664.1:p.Gln82Pro
NM_003673.4:c.245A>C MANE Select NP_003664.1:p.Gln82Pro