Canonical Allele Identifier: CA2633933909

Gene: CDH1

Linked Data

• gnomAD v4: 16-68829604-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68829604G>T , CM000678.2:g.68829604G>T	GRCh38
NC_000016.9:g.68863507G>T , CM000678.1:g.68863507G>T	GRCh37
NC_000016.8:g.67421008G>T	NCBI36
NG_008021.1:g.97313G>T , LRG_301:g.97313G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.2296-50G>T MANE Select	ENSP00000261769.4:n.2296-50G>T
ENST00000261769.9:c.2296-50G>T	ENSP00000261769.4:n.2296-50G>T
ENST00000422392.6:c.2113-50G>T	ENSP00000414946.2:n.2113-50G>T
ENST00000562118.1:n.514-50G>T
ENST00000562836.5:n.2367-50G>T
ENST00000566510.5:c.*962-50G>T	ENSP00000458139.1:n.*962-50G>T
ENST00000566612.5:c.*536-50G>T	ENSP00000454782.1:n.*536-50G>T
ENST00000611625.4:c.2359-50G>T	ENSP00000481063.1:n.2359-50G>T
ENST00000612417.4:c.1853+3050G>T	ENSP00000478360.1:n.1853+3050G>T
ENST00000621016.4:c.1866-4599G>T	ENSP00000480664.1:n.1866-4599G>T
NM_004360.3:c.2296-50G>T , LRG_301t1:c.2296-50G>T	NP_004351.1:n.2296-50G>T
XM_011523488.1:c.1561-50G>T	XP_011521790.1:n.1561-50G>T
XM_011523489.1:c.1561-50G>T	XP_011521791.1:n.1561-50G>T
NM_001317184.1:c.2113-50G>T	NP_001304113.1:n.2113-50G>T
NM_001317185.1:c.748-50G>T	NP_001304114.1:n.748-50G>T
NM_001317186.1:c.331-50G>T	NP_001304115.1:n.331-50G>T
NM_004360.4:c.2296-50G>T	NP_004351.1:n.2296-50G>T
NM_004360.5:c.2296-50G>T MANE Select	NP_004351.1:n.2296-50G>T
NM_001317184.2:c.2113-50G>T	NP_001304113.1:n.2113-50G>T
NM_001317185.2:c.748-50G>T	NP_001304114.1:n.748-50G>T
NM_001317186.2:c.331-50G>T	NP_001304115.1:n.331-50G>T