Canonical Allele Identifier: CA2633933485

Gene: CDH1

Linked Data

• gnomAD v4: 16-68834628-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68834628G>T , CM000678.2:g.68834628G>T	GRCh38
NC_000016.9:g.68868531G>T , CM000678.1:g.68868531G>T	GRCh37
NC_000016.8:g.67426032G>T	NCBI36
NG_008021.1:g.102337G>T , LRG_301:g.102337G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.*1129G>T MANE Select	ENSP00000261769.4:n.*1129G>T
ENST00000261769.9:c.*1129G>T	ENSP00000261769.4:n.*1129G>T
ENST00000566612.5:c.*2018G>T	ENSP00000454782.1:n.*2018G>T
ENST00000611625.4:c.*1129G>T	ENSP00000481063.1:n.*1129G>T
ENST00000621016.4:c.*347G>T	ENSP00000480664.1:n.*347G>T
NM_004360.3:c.*1129G>T , LRG_301t1:c.*1129G>T	NP_004351.1:n.*1129G>T
XM_011523488.1:c.*1129G>T	XP_011521790.1:n.*1129G>T
XM_011523489.1:c.*1129G>T	XP_011521791.1:n.*1129G>T
NM_001317184.1:c.*1129G>T	NP_001304113.1:n.*1129G>T
NM_001317185.1:c.*1129G>T	NP_001304114.1:n.*1129G>T
NM_001317186.1:c.*1129G>T	NP_001304115.1:n.*1129G>T
NM_004360.4:c.*1129G>T	NP_004351.1:n.*1129G>T
NM_004360.5:c.*1129G>T MANE Select	NP_004351.1:n.*1129G>T
NM_001317184.2:c.*1129G>T	NP_001304113.1:n.*1129G>T
NM_001317185.2:c.*1129G>T	NP_001304114.1:n.*1129G>T
NM_001317186.2:c.*1129G>T	NP_001304115.1:n.*1129G>T