Canonical Allele Identifier: CA157957

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68823536G>A , CM000678.2:g.68823536G>A	GRCh38
NC_000016.9:g.68857439G>A , CM000678.1:g.68857439G>A	GRCh37
NC_000016.8:g.67414940G>A	NCBI36
NG_008021.1:g.91245G>A , LRG_301:g.91245G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004360.5:c.2074G>A MANE Select	NP_004351.1:p.Ala692Thr
ENST00000261769.10:c.2074G>A MANE Select	ENSP00000261769.4:p.Ala692Thr
NM_001317184.1:c.1891G>A	NP_001304113.1:p.Ala631Thr
NM_001317184.2:c.1891G>A	NP_001304113.1:p.Ala631Thr
NM_001317185.1:c.526G>A	NP_001304114.1:p.Ala176Thr
NM_001317185.2:c.526G>A	NP_001304114.1:p.Ala176Thr
NM_001317186.1:c.109G>A	NP_001304115.1:p.Ala37Thr
NM_001317186.2:c.109G>A	NP_001304115.1:p.Ala37Thr
NM_004360.3:c.2074G>A , LRG_301t1:c.2074G>A	NP_004351.1:p.Ala692Thr
NM_004360.4:c.2074G>A	NP_004351.1:p.Ala692Thr
ENST00000261769.9:c.2074G>A	ENSP00000261769.4:p.Ala692Thr
ENST00000422392.6:c.1891G>A	ENSP00000414946.2:p.Ala631Thr
ENST00000562118.1:n.292G>A
ENST00000562836.5:n.2145G>A
ENST00000566510.5:c.*740G>A	ENSP00000458139.1:n.*740G>A
ENST00000566612.5:c.*314G>A	ENSP00000454782.1:n.*314G>A
ENST00000611625.4:c.2137G>A	ENSP00000481063.1:p.Ala713Thr
ENST00000612417.4:c.1830+1417G>A	ENSP00000478360.1:n.1830+1417G>A
ENST00000621016.4:c.1865+1382G>A	ENSP00000480664.1:n.1865+1382G>A
XM_011523488.1:c.1339G>A	XP_011521790.1:p.Ala447Thr
XM_011523489.1:c.1339G>A	XP_011521791.1:p.Ala447Thr