Canonical Allele Identifier: CA2237828965

Gene: CDH13

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.82628663G>C , CM000678.2:g.82628663G>C	GRCh38
NC_000016.9:g.82662268G>C , CM000678.1:g.82662268G>C	GRCh37
NC_000016.8:g.81219769G>C	NCBI36
NG_052819.1:g.6870G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001257.5:c.45+1526G>C MANE Select	NP_001248.1:n.45+1526G>C
ENST00000567109.6:c.45+1526G>C MANE Select	ENSP00000479395.1:n.45+1526G>C
NM_001220488.1:c.80+1526G>C	NP_001207417.1:n.80+1526G>C
NM_001220488.2:c.80+1526G>C	NP_001207417.1:n.80+1526G>C
NM_001220489.1:c.45+1526G>C	NP_001207418.1:n.45+1526G>C
NM_001220489.2:c.45+1526G>C	NP_001207418.1:n.45+1526G>C
NM_001220490.1:c.-509+1526G>C	NP_001207419.1:n.-509+1526G>C
NM_001220490.2:c.-509+1526G>C	NP_001207419.1:n.-509+1526G>C
NM_001220491.1:c.45+1526G>C	NP_001207420.1:n.45+1526G>C
NM_001220491.2:c.45+1526G>C	NP_001207420.1:n.45+1526G>C
NM_001220492.1:c.45+1526G>C	NP_001207421.1:n.45+1526G>C
NM_001220492.2:c.45+1526G>C	NP_001207421.1:n.45+1526G>C
NM_001257.4:c.45+1526G>C	NP_001248.1:n.45+1526G>C
ENST00000268613.14:c.80+1526G>C	ENSP00000268613.10:n.80+1526G>C
ENST00000428848.7:c.45+1526G>C	ENSP00000394557.3:n.45+1526G>C
ENST00000431540.7:c.45+1526G>C	ENSP00000408632.3:n.45+1526G>C
ENST00000539548.6:c.45+1526G>C	ENSP00000442225.2:n.45+1526G>C
ENST00000562601.5:c.45+1526G>C	ENSP00000455781.1:n.45+1526G>C
ENST00000565636.5:c.45+1526G>C	ENSP00000456491.1:n.45+1526G>C
ENST00000566333.1:n.167+1526G>C
ENST00000567109.5:c.45+1526G>C	ENSP00000479395.1:n.45+1526G>C
ENST00000567445.1:c.45+1526G>C	ENSP00000456297.1:n.45+1526G>C
ENST00000568770.5:c.45+1526G>C	ENSP00000457149.1:n.45+1526G>C
ENST00000569144.5:c.45+1526G>C	ENSP00000457914.1:n.45+1526G>C
ENST00000569455.1:n.99+1526G>C
XM_011522805.1:c.80+1526G>C	XP_011521107.1:n.80+1526G>C
XM_017022848.2:c.80+1526G>C	XP_016878337.1:n.80+1526G>C
XM_017022849.2:c.80+1526G>C	XP_016878338.1:n.80+1526G>C