Canonical Allele Identifier: CA285622602

Gene: CDH13

Linked Data

• dbSNP Id: rs11646411
• MyVariant Identifiers: chr16:g.82713332C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.82713332C>A , CM000678.2:g.82713332C>A	GRCh38
NC_000016.9:g.82746937C>A , CM000678.1:g.82746937C>A	GRCh37
NC_000016.8:g.81304438C>A	NCBI36
NG_052819.1:g.91539C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000567109.6:c.45+86195C>A MANE Select	ENSP00000479395.1:n.45+86195C>A
ENST00000268613.14:c.186+73867C>A	ENSP00000268613.10:n.186+73867C>A
ENST00000428848.7:c.45+86195C>A	ENSP00000394557.3:n.45+86195C>A
ENST00000431540.7:c.45+86195C>A	ENSP00000408632.3:n.45+86195C>A
ENST00000539548.6:c.45+86195C>A	ENSP00000442225.2:n.45+86195C>A
ENST00000562601.5:c.*54+8058C>A	ENSP00000455781.1:n.*54+8058C>A
ENST00000565636.5:c.45+86195C>A	ENSP00000456491.1:n.45+86195C>A
ENST00000566333.1:n.167+86195C>A
ENST00000567109.5:c.45+86195C>A	ENSP00000479395.1:n.45+86195C>A
ENST00000567445.1:c.45+86195C>A	ENSP00000456297.1:n.45+86195C>A
ENST00000568770.5:c.46-6030C>A	ENSP00000457149.1:n.46-6030C>A
ENST00000569144.5:c.45+86195C>A	ENSP00000457914.1:n.45+86195C>A
ENST00000569455.1:n.451-9689C>A
NM_001220488.1:c.186+73867C>A	NP_001207417.1:n.186+73867C>A
NM_001220489.1:c.45+86195C>A	NP_001207418.1:n.45+86195C>A
NM_001220490.1:c.-509+86195C>A	NP_001207419.1:n.-509+86195C>A
NM_001220491.1:c.45+86195C>A	NP_001207420.1:n.45+86195C>A
NM_001220492.1:c.45+86195C>A	NP_001207421.1:n.45+86195C>A
NM_001257.4:c.45+86195C>A	NP_001248.1:n.45+86195C>A
XM_011522805.1:c.186+73867C>A	XP_011521107.1:n.186+73867C>A
XR_933806.1:n.607-1601G>T
XR_933807.1:n.607-1601G>T
XM_017022848.2:c.186+73867C>A	XP_016878337.1:n.186+73867C>A
XM_017022849.2:c.186+73867C>A	XP_016878338.1:n.186+73867C>A
NM_001257.5:c.45+86195C>A MANE Select	NP_001248.1:n.45+86195C>A
NM_001220488.2:c.186+73867C>A	NP_001207417.1:n.186+73867C>A
NM_001220489.2:c.45+86195C>A	NP_001207418.1:n.45+86195C>A
NM_001220490.2:c.-509+86195C>A	NP_001207419.1:n.-509+86195C>A
NM_001220491.2:c.45+86195C>A	NP_001207420.1:n.45+86195C>A
NM_001220492.2:c.45+86195C>A	NP_001207421.1:n.45+86195C>A