Canonical Allele Identifier: CA396525326

Gene: CDH11

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.65004706C>G , CM000678.2:g.65004706C>G	GRCh38
NC_000016.9:g.65038609C>G , CM000678.1:g.65038609C>G	GRCh37
NC_000016.8:g.63596110C>G	NCBI36
NG_029491.2:g.122311G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001797.4:c.164G>C MANE Select	NP_001788.2:p.Trp55Ser
ENST00000268603.9:c.164G>C MANE Select	ENSP00000268603.4:p.Trp55Ser
NM_001308392.1:c.164G>C	NP_001295321.1:p.Trp55Ser
NM_001308392.2:c.164G>C	NP_001295321.1:p.Trp55Ser
NM_001330576.1:c.-150-5850G>C	NP_001317505.1:n.-150-5850G>C
NM_001330576.2:c.-150-5850G>C	NP_001317505.1:n.-150-5850G>C
NM_001797.2:c.164G>C	NP_001788.2:p.Trp55Ser
NM_001797.3:c.164G>C	NP_001788.2:p.Trp55Ser
ENST00000268603.8:c.164G>C	ENSP00000268603.4:p.Trp55Ser
ENST00000394156.7:c.164G>C	ENSP00000377711.3:p.Trp55Ser
ENST00000562998.1:c.164G>C	ENSP00000455420.1:p.Trp55Ser
ENST00000564317.5:c.164G>C	ENSP00000456772.1:p.Trp55Ser
ENST00000566827.5:c.-150-5850G>C	ENSP00000457812.1:n.-150-5850G>C
ENST00000567934.5:c.164G>C	ENSP00000455779.1:p.Trp55Ser
ENST00000569624.5:n.520G>C
XM_005255761.2:c.164G>C	XP_005255818.1:p.Trp55Ser
XM_005255762.1:c.164G>C	XP_005255819.1:p.Trp55Ser
XM_005255762.2:c.164G>C	XP_005255819.1:p.Trp55Ser
XM_005255763.1:c.164G>C	XP_005255820.1:p.Trp55Ser
XM_005255763.3:c.164G>C	XP_005255820.1:p.Trp55Ser
XM_011522803.1:c.164G>C	XP_011521105.1:p.Trp55Ser
XM_011522803.2:c.164G>C	XP_011521105.1:p.Trp55Ser
XM_024450134.1:c.164G>C	XP_024305902.1:p.Trp55Ser