Canonical Allele Identifier: CA2259200949

Gene: TCAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39666144C= , CM000679.2:g.39666144C=	GRCh38
NC_000017.10:g.37822397C= , CM000679.1:g.37822397C=	GRCh37
NC_000017.9:g.35075923C=	NCBI36
NG_008892.1:g.5799C= , LRG_210:g.5799C=
NG_042278.1:g.3164C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309889.3:c.*35C= MANE Select	ENSP00000312624.2:n.*35C=
ENST00000309889.2:c.*35C=	ENSP00000312624.2:n.*35C=
ENST00000578283.1:c.*35C=	ENSP00000462787.1:n.*35C=
NM_003673.3:c.*35C= , LRG_210t1:c.*35C=	NP_003664.1:n.*35C=
NM_003673.4:c.*35C= MANE Select	NP_003664.1:n.*35C=