Canonical Allele Identifier: CA2259200859

Gene: TCAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39666000A= , CM000679.2:g.39666000A=	GRCh38
NC_000017.10:g.37822253A= , CM000679.1:g.37822253A=	GRCh37
NC_000017.9:g.35075779A=	NCBI36
NG_008892.1:g.5655A= , LRG_210:g.5655A=
NG_042278.1:g.3020A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309889.3:c.395A= MANE Select	ENSP00000312624.2:p.Glu132=
ENST00000309889.2:c.395A=	ENSP00000312624.2:p.Glu132=
ENST00000578283.1:c.323A=	ENSP00000462787.1:p.Glu108=
NM_003673.3:c.395A= , LRG_210t1:c.395A=	NP_003664.1:p.Glu132=
NM_003673.4:c.395A= MANE Select	NP_003664.1:p.Glu132=