Canonical Allele Identifier: CA396457088

Gene: CDH1

Linked Data

• MyVariant Identifiers: chr16:g.68835579T>C (hg19) ; chr16:g.68801676T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68801676T>C , CM000678.2:g.68801676T>C	GRCh38
NC_000016.9:g.68835579T>C , CM000678.1:g.68835579T>C	GRCh37
NC_000016.8:g.67393080T>C	NCBI36
NG_008021.1:g.69385T>C , LRG_301:g.69385T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.170T>C MANE Select	ENSP00000261769.4:p.Phe57Ser
ENST00000261769.9:c.170T>C	ENSP00000261769.4:p.Phe57Ser
ENST00000422392.6:c.170T>C	ENSP00000414946.2:p.Phe57Ser
ENST00000562836.5:n.241T>C
ENST00000564676.5:n.452T>C
ENST00000564745.1:n.165T>C
ENST00000566510.5:c.170T>C	ENSP00000458139.1:p.Phe57Ser
ENST00000566612.5:c.170T>C	ENSP00000454782.1:p.Phe57Ser
ENST00000611625.4:c.170T>C	ENSP00000481063.1:p.Phe57Ser
ENST00000612417.4:c.170T>C	ENSP00000478360.1:p.Phe57Ser
ENST00000621016.4:c.170T>C	ENSP00000480664.1:p.Phe57Ser
NM_004360.3:c.170T>C , LRG_301t1:c.170T>C	NP_004351.1:p.Phe57Ser
XM_011523488.1:c.-566T>C	XP_011521790.1:n.-566T>C
XM_011523489.1:c.-566T>C	XP_011521791.1:n.-566T>C
NM_001317184.1:c.170T>C	NP_001304113.1:p.Phe57Ser
NM_001317185.1:c.-1446T>C	NP_001304114.1:n.-1446T>C
NM_001317186.1:c.-1650T>C	NP_001304115.1:n.-1650T>C
NM_004360.4:c.170T>C	NP_004351.1:p.Phe57Ser
NM_004360.5:c.170T>C MANE Select	NP_004351.1:p.Phe57Ser
NM_001317184.2:c.170T>C	NP_001304113.1:p.Phe57Ser
NM_001317185.2:c.-1446T>C	NP_001304114.1:n.-1446T>C
NM_001317186.2:c.-1650T>C	NP_001304115.1:n.-1650T>C