Canonical Allele Identifier: CA8092167

Gene: CDH11

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.64982005C>G , CM000678.2:g.64982005C>G	GRCh38
NC_000016.9:g.65015908C>G , CM000678.1:g.65015908C>G	GRCh37
NC_000016.8:g.63573409C>G	NCBI36
NG_029491.2:g.145012G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001797.4:c.1253+43G>C MANE Select	NP_001788.2:n.1253+43G>C
ENST00000268603.9:c.1253+43G>C MANE Select	ENSP00000268603.4:n.1253+43G>C
NM_001308392.1:c.1253+43G>C	NP_001295321.1:n.1253+43G>C
NM_001308392.2:c.1253+43G>C	NP_001295321.1:n.1253+43G>C
NM_001330576.1:c.875+43G>C	NP_001317505.1:n.875+43G>C
NM_001330576.2:c.875+43G>C	NP_001317505.1:n.875+43G>C
NM_001797.2:c.1253+43G>C	NP_001788.2:n.1253+43G>C
NM_001797.3:c.1253+43G>C	NP_001788.2:n.1253+43G>C
ENST00000268603.8:c.1253+43G>C	ENSP00000268603.4:n.1253+43G>C
ENST00000394156.7:c.1253+43G>C	ENSP00000377711.3:n.1253+43G>C
ENST00000566827.5:c.875+43G>C	ENSP00000457812.1:n.875+43G>C
XM_005255761.2:c.1253+43G>C	XP_005255818.1:n.1253+43G>C
XM_005255762.1:c.1253+43G>C	XP_005255819.1:n.1253+43G>C
XM_005255762.2:c.1253+43G>C	XP_005255819.1:n.1253+43G>C
XM_005255763.1:c.1253+43G>C	XP_005255820.1:n.1253+43G>C
XM_005255763.3:c.1253+43G>C	XP_005255820.1:n.1253+43G>C
XM_011522803.1:c.1253+43G>C	XP_011521105.1:n.1253+43G>C
XM_011522803.2:c.1253+43G>C	XP_011521105.1:n.1253+43G>C
XM_024450134.1:c.1253+43G>C	XP_024305902.1:n.1253+43G>C