Canonical Allele Identifier: CA2538920575

Gene: CDH13

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.83074109G>A , CM000678.2:g.83074109G>A	GRCh38
NC_000016.9:g.83107714G>A , CM000678.1:g.83107714G>A	GRCh37
NC_000016.8:g.81665215G>A	NCBI36
NG_052819.1:g.452316G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000567109.6:c.366+41891G>A MANE Select	ENSP00000479395.1:n.366+41891G>A
ENST00000268613.14:c.507+41891G>A	ENSP00000268613.10:n.507+41891G>A
ENST00000428848.7:c.366+41891G>A	ENSP00000394557.3:n.366+41891G>A
ENST00000431540.7:c.366+41891G>A	ENSP00000408632.3:n.366+41891G>A
ENST00000539548.6:c.158-51276G>A	ENSP00000442225.2:n.158-51276G>A
ENST00000565636.5:c.366+41891G>A	ENSP00000456491.1:n.366+41891G>A
ENST00000566620.5:c.330+41891G>A	ENSP00000454435.3:n.330+41891G>A
ENST00000567109.5:c.366+41891G>A	ENSP00000479395.1:n.366+41891G>A
ENST00000569454.1:n.283+41891G>A
ENST00000622885.4:c.327+41891G>A	ENSP00000483719.1:n.327+41891G>A
NM_001220488.1:c.507+41891G>A	NP_001207417.1:n.507+41891G>A
NM_001220489.1:c.366+41891G>A	NP_001207418.1:n.366+41891G>A
NM_001220490.1:c.-396-51276G>A	NP_001207419.1:n.-396-51276G>A
NM_001220491.1:c.366+41891G>A	NP_001207420.1:n.366+41891G>A
NM_001220492.1:c.366+41891G>A	NP_001207421.1:n.366+41891G>A
NM_001257.4:c.366+41891G>A	NP_001248.1:n.366+41891G>A
XM_011522804.1:c.63+5621G>A	XP_011521106.1:n.63+5621G>A
XM_011522805.1:c.507+41891G>A	XP_011521107.1:n.507+41891G>A
XM_011522804.3:c.63+5621G>A	XP_011521106.1:n.63+5621G>A
XM_017022848.2:c.507+41891G>A	XP_016878337.1:n.507+41891G>A
XM_017022849.2:c.507+41891G>A	XP_016878338.1:n.507+41891G>A
NM_001257.5:c.366+41891G>A MANE Select	NP_001248.1:n.366+41891G>A
NM_001220488.2:c.507+41891G>A	NP_001207417.1:n.507+41891G>A
NM_001220489.2:c.366+41891G>A	NP_001207418.1:n.366+41891G>A
NM_001220490.2:c.-396-51276G>A	NP_001207419.1:n.-396-51276G>A
NM_001220491.2:c.366+41891G>A	NP_001207420.1:n.366+41891G>A
NM_001220492.2:c.366+41891G>A	NP_001207421.1:n.366+41891G>A