Canonical Allele Identifier: CA2259200521
Gene: TCAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665412G= , CM000679.2:g.39665412G= GRCh38
NC_000017.10:g.37821665G= , CM000679.1:g.37821665G= GRCh37
NC_000017.9:g.35075191G= NCBI36
NG_008892.1:g.5067G= , LRG_210:g.5067G=
NG_042278.1:g.2432G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.3:c.53G= MANE Select ENSP00000312624.2:p.Arg18=
ENST00000309889.2:c.53G= ENSP00000312624.2:p.Arg18=
ENST00000578283.1:c.53G= ENSP00000462787.1:p.Arg18=
NM_003673.3:c.53G= , LRG_210t1:c.53G= NP_003664.1:p.Arg18=
NM_003673.4:c.53G= MANE Select NP_003664.1:p.Arg18=