Canonical Allele Identifier: CA399304546
Gene: TCAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665856C>T , CM000679.2:g.39665856C>T GRCh38
NC_000017.10:g.37822109C>T , CM000679.1:g.37822109C>T GRCh37
NC_000017.9:g.35075635C>T NCBI36
NG_008892.1:g.5511C>T , LRG_210:g.5511C>T
NG_042278.1:g.2876C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.3:c.251C>T MANE Select ENSP00000312624.2:p.Pro84Leu
ENST00000309889.2:c.251C>T ENSP00000312624.2:p.Pro84Leu
ENST00000578283.1:c.179C>T ENSP00000462787.1:p.Pro60Leu
NM_003673.3:c.251C>T , LRG_210t1:c.251C>T NP_003664.1:p.Pro84Leu
NM_003673.4:c.251C>T MANE Select NP_003664.1:p.Pro84Leu