Canonical Allele Identifier: CA2580576332

Gene: CDH13

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.83453866C= , CM000678.2:g.83453866C=	GRCh38
NC_000016.9:g.83487471C= , CM000678.1:g.83487471C=	GRCh37
NC_000016.8:g.82044972C=	NCBI36
NG_052819.1:g.832073C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001257.5:c.782-32611C= MANE Select	NP_001248.1:n.782-32611C=
ENST00000567109.6:c.782-32611C= MANE Select	ENSP00000479395.1:n.782-32611C=
NM_001220488.1:c.923-32611C=	NP_001207417.1:n.923-32611C=
NM_001220488.2:c.923-32611C=	NP_001207417.1:n.923-32611C=
NM_001220489.1:c.665-32611C=	NP_001207418.1:n.665-32611C=
NM_001220489.2:c.665-32611C=	NP_001207418.1:n.665-32611C=
NM_001220490.1:c.20-32611C=	NP_001207419.1:n.20-32611C=
NM_001220490.2:c.20-32611C=	NP_001207419.1:n.20-32611C=
NM_001257.4:c.782-32611C=	NP_001248.1:n.782-32611C=
ENST00000268613.14:c.923-32611C=	ENSP00000268613.10:n.923-32611C=
ENST00000428848.7:c.665-32611C=	ENSP00000394557.3:n.665-32611C=
ENST00000539548.6:c.*414-32611C=	ENSP00000442225.2:n.*414-32611C=
ENST00000566620.5:c.746-32611C=	ENSP00000454435.3:n.746-32611C=
ENST00000567109.5:c.782-32611C=	ENSP00000479395.1:n.782-32611C=
ENST00000569454.1:n.699-32611C=
ENST00000622885.4:c.626-32611C=	ENSP00000483719.1:n.626-32611C=
XM_011522804.1:c.479-32611C=	XP_011521106.1:n.479-32611C=
XM_011522804.3:c.479-32611C=	XP_011521106.1:n.479-32611C=
XM_011522805.1:c.923-32611C=	XP_011521107.1:n.923-32611C=
XM_017022848.2:c.923-32611C=	XP_016878337.1:n.923-32611C=