Canonical Allele Identifier: CA2259200868

Gene: TCAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39666027C= , CM000679.2:g.39666027C=	GRCh38
NC_000017.10:g.37822280C= , CM000679.1:g.37822280C=	GRCh37
NC_000017.9:g.35075806C=	NCBI36
NG_008892.1:g.5682C= , LRG_210:g.5682C=
NG_042278.1:g.3047C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309889.3:c.422C= MANE Select	ENSP00000312624.2:p.Pro141=
ENST00000309889.2:c.422C=	ENSP00000312624.2:p.Pro141=
ENST00000578283.1:c.350C=	ENSP00000462787.1:p.Pro117=
NM_003673.3:c.422C= , LRG_210t1:c.422C=	NP_003664.1:p.Pro141=
NM_003673.4:c.422C= MANE Select	NP_003664.1:p.Pro141=