Canonical Allele Identifier: CA2259200878

Gene: TCAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39666044A= , CM000679.2:g.39666044A=	GRCh38
NC_000017.10:g.37822297A= , CM000679.1:g.37822297A=	GRCh37
NC_000017.9:g.35075823A=	NCBI36
NG_008892.1:g.5699A= , LRG_210:g.5699A=
NG_042278.1:g.3064A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309889.3:c.439A= MANE Select	ENSP00000312624.2:p.Ser147=
ENST00000309889.2:c.439A=	ENSP00000312624.2:p.Ser147=
ENST00000578283.1:c.367A=	ENSP00000462787.1:p.Ser123=
NM_003673.3:c.439A= , LRG_210t1:c.439A=	NP_003664.1:p.Ser147=
NM_003673.4:c.439A= MANE Select	NP_003664.1:p.Ser147=