Canonical Allele Identifier: CA2259200517
Gene: TCAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665409G= , CM000679.2:g.39665409G= GRCh38
NC_000017.10:g.37821662G= , CM000679.1:g.37821662G= GRCh37
NC_000017.9:g.35075188G= NCBI36
NG_008892.1:g.5064G= , LRG_210:g.5064G=
NG_042278.1:g.2429G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.3:c.50G= MANE Select ENSP00000312624.2:p.Arg17=
ENST00000309889.2:c.50G= ENSP00000312624.2:p.Arg17=
ENST00000578283.1:c.50G= ENSP00000462787.1:p.Arg17=
NM_003673.3:c.50G= , LRG_210t1:c.50G= NP_003664.1:p.Arg17=
NM_003673.4:c.50G= MANE Select NP_003664.1:p.Arg17=