Canonical Allele Identifier: CA2259200806

Gene: TCAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39665899G= , CM000679.2:g.39665899G=	GRCh38
NC_000017.10:g.37822152G= , CM000679.1:g.37822152G=	GRCh37
NC_000017.9:g.35075678G=	NCBI36
NG_008892.1:g.5554G= , LRG_210:g.5554G=
NG_042278.1:g.2919G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309889.3:c.294G= MANE Select	ENSP00000312624.2:p.Lys98=
ENST00000309889.2:c.294G=	ENSP00000312624.2:p.Lys98=
ENST00000578283.1:c.222G=	ENSP00000462787.1:p.Lys74=
NM_003673.3:c.294G= , LRG_210t1:c.294G=	NP_003664.1:p.Lys98=
NM_003673.4:c.294G= MANE Select	NP_003664.1:p.Lys98=