Canonical Allele Identifier: CA2259200653
Gene: TCAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665768G= , CM000679.2:g.39665768G= GRCh38
NC_000017.10:g.37822021G= , CM000679.1:g.37822021G= GRCh37
NC_000017.9:g.35075547G= NCBI36
NG_008892.1:g.5423G= , LRG_210:g.5423G=
NG_042278.1:g.2788G=

Transcript Alleles

HGVS Amino-acid change
ENST00000309889.3:c.163G= MANE Select ENSP00000312624.2:p.Gly55=
ENST00000309889.2:c.163G= ENSP00000312624.2:p.Gly55=
ENST00000578283.1:c.163G= ENSP00000462787.1:p.Gly55=
NM_003673.3:c.163G= , LRG_210t1:c.163G= NP_003664.1:p.Gly55=
NM_003673.4:c.163G= MANE Select NP_003664.1:p.Gly55=