Canonical Allele Identifier: CA2238127136

Gene: CDH13

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.83678830A= , CM000678.2:g.83678830A=	GRCh38
NC_000016.9:g.83712435A= , CM000678.1:g.83712435A=	GRCh37
NC_000016.8:g.82269936A=	NCBI36
NG_052819.1:g.1057037A=

Transcript Alleles

HGVS	Amino-acid Change
NM_001257.5:c.1538+369A= MANE Select	NP_001248.1:n.1538+369A=
ENST00000567109.6:c.1538+369A= MANE Select	ENSP00000479395.1:n.1538+369A=
NM_001220488.1:c.1679+369A=	NP_001207417.1:n.1679+369A=
NM_001220488.2:c.1679+369A=	NP_001207417.1:n.1679+369A=
NM_001220489.1:c.1421+369A=	NP_001207418.1:n.1421+369A=
NM_001220489.2:c.1421+369A=	NP_001207418.1:n.1421+369A=
NM_001220490.1:c.776+369A=	NP_001207419.1:n.776+369A=
NM_001220490.2:c.776+369A=	NP_001207419.1:n.776+369A=
NM_001257.4:c.1538+369A=	NP_001248.1:n.1538+369A=
ENST00000268613.14:c.1679+369A=	ENSP00000268613.10:n.1679+369A=
ENST00000428848.7:c.1421+369A=	ENSP00000394557.3:n.1421+369A=
ENST00000539548.6:c.*1170+369A=	ENSP00000442225.2:n.*1170+369A=
ENST00000566620.5:c.1502+369A=	ENSP00000454435.3:n.1502+369A=
ENST00000567109.5:c.1538+369A=	ENSP00000479395.1:n.1538+369A=
ENST00000615627.1:c.458+369A=	ENSP00000482651.1:n.458+369A=
ENST00000622885.4:c.1382+369A=	ENSP00000483719.1:n.1382+369A=
XM_011522804.1:c.1235+369A=	XP_011521106.1:n.1235+369A=
XM_011522804.3:c.1235+369A=	XP_011521106.1:n.1235+369A=
XR_001752385.2:n.6466-11239T=