Canonical Allele Identifier: CA2580576330

Gene: CDH13

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.83250733G= , CM000678.2:g.83250733G=	GRCh38
NC_000016.9:g.83284338G= , CM000678.1:g.83284338G=	GRCh37
NC_000016.8:g.81841839G=	NCBI36
NG_052819.1:g.628940G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001257.5:c.636+33236G= MANE Select	NP_001248.1:n.636+33236G=
ENST00000567109.6:c.636+33236G= MANE Select	ENSP00000479395.1:n.636+33236G=
NM_001220488.1:c.777+33236G=	NP_001207417.1:n.777+33236G=
NM_001220488.2:c.777+33236G=	NP_001207417.1:n.777+33236G=
NM_001220489.1:c.519+33236G=	NP_001207418.1:n.519+33236G=
NM_001220489.2:c.519+33236G=	NP_001207418.1:n.519+33236G=
NM_001220490.1:c.-127+33236G=	NP_001207419.1:n.-127+33236G=
NM_001220490.2:c.-127+33236G=	NP_001207419.1:n.-127+33236G=
NM_001257.4:c.636+33236G=	NP_001248.1:n.636+33236G=
ENST00000268613.14:c.777+33236G=	ENSP00000268613.10:n.777+33236G=
ENST00000428848.7:c.519+33236G=	ENSP00000394557.3:n.519+33236G=
ENST00000539548.6:c.*268+33236G=	ENSP00000442225.2:n.*268+33236G=
ENST00000566620.5:c.600+33236G=	ENSP00000454435.3:n.600+33236G=
ENST00000567109.5:c.636+33236G=	ENSP00000479395.1:n.636+33236G=
ENST00000569454.1:n.553+33236G=
ENST00000622885.4:c.480+33236G=	ENSP00000483719.1:n.480+33236G=
XM_011522804.1:c.333+33236G=	XP_011521106.1:n.333+33236G=
XM_011522804.3:c.333+33236G=	XP_011521106.1:n.333+33236G=
XM_011522805.1:c.777+33236G=	XP_011521107.1:n.777+33236G=
XM_017022848.2:c.777+33236G=	XP_016878337.1:n.777+33236G=