Canonical Allele Identifier: CA2581278938

Gene: CDH13

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.83493987G= , CM000678.2:g.83493987G=	GRCh38
NC_000016.9:g.83527592G= , CM000678.1:g.83527592G=	GRCh37
NC_000016.8:g.82085093G=	NCBI36
NG_052819.1:g.872194G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567109.6:c.960+7332G= MANE Select	ENSP00000479395.1:n.960+7332G=
ENST00000268613.14:c.1101+7332G=	ENSP00000268613.10:n.1101+7332G=
ENST00000428848.7:c.843+7332G=	ENSP00000394557.3:n.843+7332G=
ENST00000539548.6:c.*592+7332G=	ENSP00000442225.2:n.*592+7332G=
ENST00000566620.5:c.924+7332G=	ENSP00000454435.3:n.924+7332G=
ENST00000567109.5:c.960+7332G=	ENSP00000479395.1:n.960+7332G=
ENST00000622885.4:c.804+7332G=	ENSP00000483719.1:n.804+7332G=
NM_001220488.1:c.1101+7332G=	NP_001207417.1:n.1101+7332G=
NM_001220489.1:c.843+7332G=	NP_001207418.1:n.843+7332G=
NM_001220490.1:c.198+7332G=	NP_001207419.1:n.198+7332G=
NM_001257.4:c.960+7332G=	NP_001248.1:n.960+7332G=
XM_011522804.1:c.657+7332G=	XP_011521106.1:n.657+7332G=
XM_011522805.1:c.1101+7332G=	XP_011521107.1:n.1101+7332G=
XM_011522804.3:c.657+7332G=	XP_011521106.1:n.657+7332G=
XM_017022848.2:c.1101+7332G=	XP_016878337.1:n.1101+7332G=
NM_001257.5:c.960+7332G= MANE Select	NP_001248.1:n.960+7332G=
NM_001220488.2:c.1101+7332G=	NP_001207417.1:n.1101+7332G=
NM_001220489.2:c.843+7332G=	NP_001207418.1:n.843+7332G=
NM_001220490.2:c.198+7332G=	NP_001207419.1:n.198+7332G=