Canonical Allele Identifier: CA2732590679

Gene: CDH1

Linked Data

• dbSNP Id: rs953094555

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68823644G>C , CM000678.2:g.68823644G>C	GRCh38
NC_000016.9:g.68857547G>C , CM000678.1:g.68857547G>C	GRCh37
NC_000016.8:g.67415048G>C	NCBI36
NG_008021.1:g.91353G>C , LRG_301:g.91353G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.2164+18G>C MANE Select	ENSP00000261769.4:n.2164+18G>C
ENST00000261769.9:c.2164+18G>C	ENSP00000261769.4:n.2164+18G>C
ENST00000422392.6:c.1981+18G>C	ENSP00000414946.2:n.1981+18G>C
ENST00000562118.1:n.382+18G>C
ENST00000562836.5:n.2235+18G>C
ENST00000566510.5:c.*830+18G>C	ENSP00000458139.1:n.*830+18G>C
ENST00000566612.5:c.*404+18G>C	ENSP00000454782.1:n.*404+18G>C
ENST00000611625.4:c.2227+18G>C	ENSP00000481063.1:n.2227+18G>C
ENST00000612417.4:c.1830+1525G>C	ENSP00000478360.1:n.1830+1525G>C
ENST00000621016.4:c.1865+1490G>C	ENSP00000480664.1:n.1865+1490G>C
NM_004360.3:c.2164+18G>C , LRG_301t1:c.2164+18G>C	NP_004351.1:n.2164+18G>C
XM_011523488.1:c.1429+18G>C	XP_011521790.1:n.1429+18G>C
XM_011523489.1:c.1429+18G>C	XP_011521791.1:n.1429+18G>C
NM_001317184.1:c.1981+18G>C	NP_001304113.1:n.1981+18G>C
NM_001317185.1:c.616+18G>C	NP_001304114.1:n.616+18G>C
NM_001317186.1:c.199+18G>C	NP_001304115.1:n.199+18G>C
NM_004360.4:c.2164+18G>C	NP_004351.1:n.2164+18G>C
NM_004360.5:c.2164+18G>C MANE Select	NP_004351.1:n.2164+18G>C
NM_001317184.2:c.1981+18G>C	NP_001304113.1:n.1981+18G>C
NM_001317185.2:c.616+18G>C	NP_001304114.1:n.616+18G>C
NM_001317186.2:c.199+18G>C	NP_001304115.1:n.199+18G>C