Canonical Allele Identifier: CA2633932191

Gene: CDH1

Linked Data

• gnomAD v4: 16-68833269-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68833269C>A , CM000678.2:g.68833269C>A	GRCh38
NC_000016.9:g.68867172C>A , CM000678.1:g.68867172C>A	GRCh37
NC_000016.8:g.67424673C>A	NCBI36
NG_008021.1:g.100978C>A , LRG_301:g.100978C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.2440-21C>A MANE Select	ENSP00000261769.4:n.2440-21C>A
ENST00000261769.9:c.2440-21C>A	ENSP00000261769.4:n.2440-21C>A
ENST00000422392.6:c.2257-21C>A	ENSP00000414946.2:n.2257-21C>A
ENST00000562118.1:n.658-21C>A
ENST00000562836.5:n.2511-21C>A
ENST00000566510.5:c.*1106-21C>A	ENSP00000458139.1:n.*1106-21C>A
ENST00000566612.5:c.*680-21C>A	ENSP00000454782.1:n.*680-21C>A
ENST00000611625.4:c.2503-21C>A	ENSP00000481063.1:n.2503-21C>A
ENST00000612417.4:c.1854-922C>A	ENSP00000478360.1:n.1854-922C>A
ENST00000621016.4:c.1866-934C>A	ENSP00000480664.1:n.1866-934C>A
NM_004360.3:c.2440-21C>A , LRG_301t1:c.2440-21C>A	NP_004351.1:n.2440-21C>A
XM_011523488.1:c.1705-21C>A	XP_011521790.1:n.1705-21C>A
XM_011523489.1:c.1705-21C>A	XP_011521791.1:n.1705-21C>A
NM_001317184.1:c.2257-21C>A	NP_001304113.1:n.2257-21C>A
NM_001317185.1:c.892-21C>A	NP_001304114.1:n.892-21C>A
NM_001317186.1:c.475-21C>A	NP_001304115.1:n.475-21C>A
NM_004360.4:c.2440-21C>A	NP_004351.1:n.2440-21C>A
NM_004360.5:c.2440-21C>A MANE Select	NP_004351.1:n.2440-21C>A
NM_001317184.2:c.2257-21C>A	NP_001304113.1:n.2257-21C>A
NM_001317185.2:c.892-21C>A	NP_001304114.1:n.892-21C>A
NM_001317186.2:c.475-21C>A	NP_001304115.1:n.475-21C>A