Canonical Allele Identifier: CA2732908677

Gene: CDH1

Linked Data

• dbSNP Id: rs2152113849

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68737340A>T , CM000678.2:g.68737340A>T	GRCh38
NC_000016.9:g.68771243A>T , CM000678.1:g.68771243A>T	GRCh37
NC_000016.8:g.67328744A>T	NCBI36
NG_008021.1:g.5049A>T , LRG_301:g.5049A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.-76A>T MANE Select	ENSP00000261769.4:n.-76A>T
ENST00000261769.9:c.-76A>T	ENSP00000261769.4:n.-76A>T
ENST00000566612.5:c.-76A>T	ENSP00000454782.1:n.-76A>T
ENST00000611625.4:c.-76A>T	ENSP00000481063.1:n.-76A>T
ENST00000612417.4:c.-76A>T	ENSP00000478360.1:n.-76A>T
ENST00000621016.4:c.-76A>T	ENSP00000480664.1:n.-76A>T
NM_004360.3:c.-76A>T , LRG_301t1:c.-76A>T	NP_004351.1:n.-76A>T
NM_001317184.1:c.-76A>T	NP_001304113.1:n.-76A>T
NM_001317185.1:c.-1691A>T	NP_001304114.1:n.-1691A>T
NM_001317186.1:c.-1895A>T	NP_001304115.1:n.-1895A>T
NM_004360.4:c.-76A>T	NP_004351.1:n.-76A>T
NM_004360.5:c.-76A>T MANE Select	NP_004351.1:n.-76A>T
NM_001317184.2:c.-76A>T	NP_001304113.1:n.-76A>T
NM_001317185.2:c.-1691A>T	NP_001304114.1:n.-1691A>T
NM_001317186.2:c.-1895A>T	NP_001304115.1:n.-1895A>T