Canonical Allele Identifier: CA2633897194

Gene: CDH1

Linked Data

• gnomAD v4: 16-68737299-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68737299T>G , CM000678.2:g.68737299T>G	GRCh38
NC_000016.9:g.68771202T>G , CM000678.1:g.68771202T>G	GRCh37
NC_000016.8:g.67328703T>G	NCBI36
NG_008021.1:g.5008T>G , LRG_301:g.5008T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.-117T>G MANE Select	ENSP00000261769.4:n.-117T>G
ENST00000261769.9:c.-117T>G	ENSP00000261769.4:n.-117T>G
ENST00000611625.4:c.-117T>G	ENSP00000481063.1:n.-117T>G
ENST00000612417.4:c.-117T>G	ENSP00000478360.1:n.-117T>G
NM_004360.3:c.-117T>G , LRG_301t1:c.-117T>G	NP_004351.1:n.-117T>G
NM_001317184.1:c.-117T>G	NP_001304113.1:n.-117T>G
NM_001317185.1:c.-1732T>G	NP_001304114.1:n.-1732T>G
NM_001317186.1:c.-1936T>G	NP_001304115.1:n.-1936T>G
NM_004360.4:c.-117T>G	NP_004351.1:n.-117T>G
NM_004360.5:c.-117T>G MANE Select	NP_004351.1:n.-117T>G
NM_001317184.2:c.-117T>G	NP_001304113.1:n.-117T>G
NM_001317185.2:c.-1732T>G	NP_001304114.1:n.-1732T>G
NM_001317186.2:c.-1936T>G	NP_001304115.1:n.-1936T>G