Canonical Allele Identifier: CA496153952

Gene: CDH1

Linked Data

• gnomAD v4: 16-68815580-T-C
• MyVariant Identifiers: chr16:g.68849483T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68815580T>C , CM000678.2:g.68815580T>C	GRCh38
NC_000016.9:g.68849483T>C , CM000678.1:g.68849483T>C	GRCh37
NC_000016.8:g.67406984T>C	NCBI36
NG_008021.1:g.83289T>C , LRG_301:g.83289T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.1386T>C MANE Select	ENSP00000261769.4:p.Phe462=
ENST00000261769.9:c.1386T>C	ENSP00000261769.4:p.Phe462=
ENST00000422392.6:c.1203T>C	ENSP00000414946.2:p.Phe401=
ENST00000562836.5:n.1457T>C
ENST00000566510.5:c.*52T>C	ENSP00000458139.1:n.*52T>C
ENST00000566612.5:c.1386T>C	ENSP00000454782.1:p.Phe462=
ENST00000611625.4:c.1449T>C	ENSP00000481063.1:p.Phe483=
ENST00000612417.4:c.1386T>C	ENSP00000478360.1:p.Phe462=
ENST00000621016.4:c.1386T>C	ENSP00000480664.1:p.Phe462=
NM_004360.3:c.1386T>C , LRG_301t1:c.1386T>C	NP_004351.1:p.Phe462=
XM_011523488.1:c.651T>C	XP_011521790.1:p.Phe217=
XM_011523489.1:c.651T>C	XP_011521791.1:p.Phe217=
NM_001317184.1:c.1203T>C	NP_001304113.1:p.Phe401=
NM_001317185.1:c.-163T>C	NP_001304114.1:n.-163T>C
NM_001317186.1:c.-434T>C	NP_001304115.1:n.-434T>C
NM_004360.4:c.1386T>C	NP_004351.1:p.Phe462=
NM_004360.5:c.1386T>C MANE Select	NP_004351.1:p.Phe462=
NM_001317184.2:c.1203T>C	NP_001304113.1:p.Phe401=
NM_001317185.2:c.-163T>C	NP_001304114.1:n.-163T>C
NM_001317186.2:c.-434T>C	NP_001304115.1:n.-434T>C