Canonical Allele Identifier: CA396458872

Gene: CDH1

Linked Data

• dbSNP Id: rs750979600
• gnomAD v4: 16-68810314-G-C
• MyVariant Identifiers: chr16:g.68844217G>C (hg19) ; chr16:g.68810314G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68810314G>C , CM000678.2:g.68810314G>C	GRCh38
NC_000016.9:g.68844217G>C , CM000678.1:g.68844217G>C	GRCh37
NC_000016.8:g.67401718G>C	NCBI36
NG_008021.1:g.78023G>C , LRG_301:g.78023G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.805G>C MANE Select	ENSP00000261769.4:p.Gly269Arg
ENST00000261769.9:c.805G>C	ENSP00000261769.4:p.Gly269Arg
ENST00000422392.6:c.805G>C	ENSP00000414946.2:p.Gly269Arg
ENST00000561751.1:c.455-1370G>C
ENST00000562836.5:n.876G>C
ENST00000566510.5:c.649G>C	ENSP00000458139.1:p.Gly217Arg
ENST00000566612.5:c.805G>C	ENSP00000454782.1:p.Gly269Arg
ENST00000611625.4:c.805G>C	ENSP00000481063.1:p.Gly269Arg
ENST00000612417.4:c.805G>C	ENSP00000478360.1:p.Gly269Arg
ENST00000621016.4:c.805G>C	ENSP00000480664.1:p.Gly269Arg
NM_004360.3:c.805G>C , LRG_301t1:c.805G>C	NP_004351.1:p.Gly269Arg
XM_011523488.1:c.70G>C	XP_011521790.1:p.Gly24Arg
XM_011523489.1:c.70G>C	XP_011521791.1:p.Gly24Arg
NM_001317184.1:c.805G>C	NP_001304113.1:p.Gly269Arg
NM_001317185.1:c.-811G>C	NP_001304114.1:n.-811G>C
NM_001317186.1:c.-1015G>C	NP_001304115.1:n.-1015G>C
NM_004360.4:c.805G>C	NP_004351.1:p.Gly269Arg
NM_004360.5:c.805G>C MANE Select	NP_004351.1:p.Gly269Arg
NM_001317184.2:c.805G>C	NP_001304113.1:p.Gly269Arg
NM_001317185.2:c.-811G>C	NP_001304114.1:n.-811G>C
NM_001317186.2:c.-1015G>C	NP_001304115.1:n.-1015G>C