Canonical Allele Identifier: CA2633899902

Gene: CDH1

Linked Data

• gnomAD v4: 16-68810372-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68810372A>G , CM000678.2:g.68810372A>G	GRCh38
NC_000016.9:g.68844275A>G , CM000678.1:g.68844275A>G	GRCh37
NC_000016.8:g.67401776A>G	NCBI36
NG_008021.1:g.78081A>G , LRG_301:g.78081A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.832+31A>G MANE Select	ENSP00000261769.4:n.832+31A>G
ENST00000261769.9:c.832+31A>G	ENSP00000261769.4:n.832+31A>G
ENST00000422392.6:c.832+31A>G	ENSP00000414946.2:n.832+31A>G
ENST00000561751.1:c.455-1312A>G
ENST00000562836.5:n.903+31A>G
ENST00000566510.5:c.676+31A>G	ENSP00000458139.1:n.676+31A>G
ENST00000566612.5:c.832+31A>G	ENSP00000454782.1:n.832+31A>G
ENST00000611625.4:c.832+31A>G	ENSP00000481063.1:n.832+31A>G
ENST00000612417.4:c.832+31A>G	ENSP00000478360.1:n.832+31A>G
ENST00000621016.4:c.832+31A>G	ENSP00000480664.1:n.832+31A>G
NM_004360.3:c.832+31A>G , LRG_301t1:c.832+31A>G	NP_004351.1:n.832+31A>G
XM_011523488.1:c.97+31A>G	XP_011521790.1:n.97+31A>G
XM_011523489.1:c.97+31A>G	XP_011521791.1:n.97+31A>G
NM_001317184.1:c.832+31A>G	NP_001304113.1:n.832+31A>G
NM_001317185.1:c.-784+31A>G	NP_001304114.1:n.-784+31A>G
NM_001317186.1:c.-988+31A>G	NP_001304115.1:n.-988+31A>G
NM_004360.4:c.832+31A>G	NP_004351.1:n.832+31A>G
NM_004360.5:c.832+31A>G MANE Select	NP_004351.1:n.832+31A>G
NM_001317184.2:c.832+31A>G	NP_001304113.1:n.832+31A>G
NM_001317185.2:c.-784+31A>G	NP_001304114.1:n.-784+31A>G
NM_001317186.2:c.-988+31A>G	NP_001304115.1:n.-988+31A>G