Canonical Allele Identifier: CA2237868541

Gene: CDH13

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.82713332C= , CM000678.2:g.82713332C=	GRCh38
NC_000016.9:g.82746937C= , CM000678.1:g.82746937C=	GRCh37
NC_000016.8:g.81304438C=	NCBI36
NG_052819.1:g.91539C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001257.5:c.45+86195C= MANE Select	NP_001248.1:n.45+86195C=
ENST00000567109.6:c.45+86195C= MANE Select	ENSP00000479395.1:n.45+86195C=
NM_001220488.1:c.186+73867C=	NP_001207417.1:n.186+73867C=
NM_001220488.2:c.186+73867C=	NP_001207417.1:n.186+73867C=
NM_001220489.1:c.45+86195C=	NP_001207418.1:n.45+86195C=
NM_001220489.2:c.45+86195C=	NP_001207418.1:n.45+86195C=
NM_001220490.1:c.-509+86195C=	NP_001207419.1:n.-509+86195C=
NM_001220490.2:c.-509+86195C=	NP_001207419.1:n.-509+86195C=
NM_001220491.1:c.45+86195C=	NP_001207420.1:n.45+86195C=
NM_001220491.2:c.45+86195C=	NP_001207420.1:n.45+86195C=
NM_001220492.1:c.45+86195C=	NP_001207421.1:n.45+86195C=
NM_001220492.2:c.45+86195C=	NP_001207421.1:n.45+86195C=
NM_001257.4:c.45+86195C=	NP_001248.1:n.45+86195C=
ENST00000268613.14:c.186+73867C=	ENSP00000268613.10:n.186+73867C=
ENST00000428848.7:c.45+86195C=	ENSP00000394557.3:n.45+86195C=
ENST00000431540.7:c.45+86195C=	ENSP00000408632.3:n.45+86195C=
ENST00000539548.6:c.45+86195C=	ENSP00000442225.2:n.45+86195C=
ENST00000562601.5:c.*54+8058C=	ENSP00000455781.1:n.*54+8058C=
ENST00000565636.5:c.45+86195C=	ENSP00000456491.1:n.45+86195C=
ENST00000566333.1:n.167+86195C=
ENST00000567109.5:c.45+86195C=	ENSP00000479395.1:n.45+86195C=
ENST00000567445.1:c.45+86195C=	ENSP00000456297.1:n.45+86195C=
ENST00000568770.5:c.46-6030C=	ENSP00000457149.1:n.46-6030C=
ENST00000569144.5:c.45+86195C=	ENSP00000457914.1:n.45+86195C=
ENST00000569455.1:n.451-9689C=
XM_011522805.1:c.186+73867C=	XP_011521107.1:n.186+73867C=
XM_017022848.2:c.186+73867C=	XP_016878337.1:n.186+73867C=
XM_017022849.2:c.186+73867C=	XP_016878338.1:n.186+73867C=
XR_933806.1:n.607-1601G=
XR_933807.1:n.607-1601G=