Canonical Allele Identifier: CA2732908355

Gene: CDH1

Linked Data

• dbSNP Id: rs2152113841

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68737330A>G , CM000678.2:g.68737330A>G	GRCh38
NC_000016.9:g.68771233A>G , CM000678.1:g.68771233A>G	GRCh37
NC_000016.8:g.67328734A>G	NCBI36
NG_008021.1:g.5039A>G , LRG_301:g.5039A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.-86A>G MANE Select	ENSP00000261769.4:n.-86A>G
ENST00000261769.9:c.-86A>G	ENSP00000261769.4:n.-86A>G
ENST00000566612.5:c.-86A>G	ENSP00000454782.1:n.-86A>G
ENST00000611625.4:c.-86A>G	ENSP00000481063.1:n.-86A>G
ENST00000612417.4:c.-86A>G	ENSP00000478360.1:n.-86A>G
ENST00000621016.4:c.-86A>G	ENSP00000480664.1:n.-86A>G
NM_004360.3:c.-86A>G , LRG_301t1:c.-86A>G	NP_004351.1:n.-86A>G
NM_001317184.1:c.-86A>G	NP_001304113.1:n.-86A>G
NM_001317185.1:c.-1701A>G	NP_001304114.1:n.-1701A>G
NM_001317186.1:c.-1905A>G	NP_001304115.1:n.-1905A>G
NM_004360.4:c.-86A>G	NP_004351.1:n.-86A>G
NM_004360.5:c.-86A>G MANE Select	NP_004351.1:n.-86A>G
NM_001317184.2:c.-86A>G	NP_001304113.1:n.-86A>G
NM_001317185.2:c.-1701A>G	NP_001304114.1:n.-1701A>G
NM_001317186.2:c.-1905A>G	NP_001304115.1:n.-1905A>G