Canonical Allele Identifier: CA2581278694

Gene: CDH13

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.83178793G= , CM000678.2:g.83178793G=	GRCh38
NC_000016.9:g.83212398G= , CM000678.1:g.83212398G=	GRCh37
NC_000016.8:g.81769899G=	NCBI36
NG_052819.1:g.557000G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001257.5:c.484-38552G= MANE Select	NP_001248.1:n.484-38552G=
ENST00000567109.6:c.484-38552G= MANE Select	ENSP00000479395.1:n.484-38552G=
NM_001220488.1:c.625-38552G=	NP_001207417.1:n.625-38552G=
NM_001220488.2:c.625-38552G=	NP_001207417.1:n.625-38552G=
NM_001220489.1:c.367-38552G=	NP_001207418.1:n.367-38552G=
NM_001220489.2:c.367-38552G=	NP_001207418.1:n.367-38552G=
NM_001220490.1:c.-279-38552G=	NP_001207419.1:n.-279-38552G=
NM_001220490.2:c.-279-38552G=	NP_001207419.1:n.-279-38552G=
NM_001220491.1:c.484-2077G=	NP_001207420.1:n.484-2077G=
NM_001220491.2:c.484-2077G=	NP_001207420.1:n.484-2077G=
NM_001220492.1:c.*2-2075G=	NP_001207421.1:n.*2-2075G=
NM_001220492.2:c.*2-2075G=	NP_001207421.1:n.*2-2075G=
NM_001257.4:c.484-38552G=	NP_001248.1:n.484-38552G=
ENST00000268613.14:c.625-38552G=	ENSP00000268613.10:n.625-38552G=
ENST00000428848.7:c.367-38552G=	ENSP00000394557.3:n.367-38552G=
ENST00000431540.7:c.484-2077G=	ENSP00000408632.3:n.484-2077G=
ENST00000539548.6:c.*116-38552G=	ENSP00000442225.2:n.*116-38552G=
ENST00000565636.5:c.*6-2079G=	ENSP00000456491.1:n.*6-2079G=
ENST00000566620.5:c.448-38552G=	ENSP00000454435.3:n.448-38552G=
ENST00000567109.5:c.484-38552G=	ENSP00000479395.1:n.484-38552G=
ENST00000569454.1:n.401-38552G=
ENST00000622885.4:c.328-38552G=	ENSP00000483719.1:n.328-38552G=
XM_011522804.1:c.181-38552G=	XP_011521106.1:n.181-38552G=
XM_011522804.3:c.181-38552G=	XP_011521106.1:n.181-38552G=
XM_011522805.1:c.625-38552G=	XP_011521107.1:n.625-38552G=
XM_017022848.2:c.625-38552G=	XP_016878337.1:n.625-38552G=
XM_017022849.2:c.625-2077G=	XP_016878338.1:n.625-2077G=