Canonical Allele Identifier: CA2633897219

Gene: CDH1

Linked Data

• gnomAD v4: 16-68737306-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68737306T>C , CM000678.2:g.68737306T>C	GRCh38
NC_000016.9:g.68771209T>C , CM000678.1:g.68771209T>C	GRCh37
NC_000016.8:g.67328710T>C	NCBI36
NG_008021.1:g.5015T>C , LRG_301:g.5015T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.-110T>C MANE Select	ENSP00000261769.4:n.-110T>C
ENST00000261769.9:c.-110T>C	ENSP00000261769.4:n.-110T>C
ENST00000611625.4:c.-110T>C	ENSP00000481063.1:n.-110T>C
ENST00000612417.4:c.-110T>C	ENSP00000478360.1:n.-110T>C
NM_004360.3:c.-110T>C , LRG_301t1:c.-110T>C	NP_004351.1:n.-110T>C
NM_001317184.1:c.-110T>C	NP_001304113.1:n.-110T>C
NM_001317185.1:c.-1725T>C	NP_001304114.1:n.-1725T>C
NM_001317186.1:c.-1929T>C	NP_001304115.1:n.-1929T>C
NM_004360.4:c.-110T>C	NP_004351.1:n.-110T>C
NM_004360.5:c.-110T>C MANE Select	NP_004351.1:n.-110T>C
NM_001317184.2:c.-110T>C	NP_001304113.1:n.-110T>C
NM_001317185.2:c.-1725T>C	NP_001304114.1:n.-1725T>C
NM_001317186.2:c.-1929T>C	NP_001304115.1:n.-1929T>C