Canonical Allele Identifier: CA2807902223

Gene: CDH13

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.83676132C>A , CM000678.2:g.83676132C>A	GRCh38
NC_000016.9:g.83709737C>A , CM000678.1:g.83709737C>A	GRCh37
NC_000016.8:g.82267238C>A	NCBI36
NG_052819.1:g.1054339C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567109.6:c.1285-2076C>A MANE Select	ENSP00000479395.1:n.1285-2076C>A
ENST00000268613.14:c.1426-2076C>A	ENSP00000268613.10:n.1426-2076C>A
ENST00000428848.7:c.1168-2076C>A	ENSP00000394557.3:n.1168-2076C>A
ENST00000539548.6:c.*917-2076C>A	ENSP00000442225.2:n.*917-2076C>A
ENST00000566620.5:c.1249-2076C>A	ENSP00000454435.3:n.1249-2076C>A
ENST00000567109.5:c.1285-2076C>A	ENSP00000479395.1:n.1285-2076C>A
ENST00000615627.1:c.205-2076C>A	ENSP00000482651.1:n.205-2076C>A
ENST00000622885.4:c.1129-2076C>A	ENSP00000483719.1:n.1129-2076C>A
NM_001220488.1:c.1426-2076C>A	NP_001207417.1:n.1426-2076C>A
NM_001220489.1:c.1168-2076C>A	NP_001207418.1:n.1168-2076C>A
NM_001220490.1:c.523-2076C>A	NP_001207419.1:n.523-2076C>A
NM_001257.4:c.1285-2076C>A	NP_001248.1:n.1285-2076C>A
XM_011522804.1:c.982-2076C>A	XP_011521106.1:n.982-2076C>A
XM_011522804.3:c.982-2076C>A	XP_011521106.1:n.982-2076C>A
XR_001752385.2:n.6466-8541G>T
NM_001257.5:c.1285-2076C>A MANE Select	NP_001248.1:n.1285-2076C>A
NM_001220488.2:c.1426-2076C>A	NP_001207417.1:n.1426-2076C>A
NM_001220489.2:c.1168-2076C>A	NP_001207418.1:n.1168-2076C>A
NM_001220490.2:c.523-2076C>A	NP_001207419.1:n.523-2076C>A