Canonical Allele Identifier: CA496393046

Gene: CDH1

Linked Data

• MyVariant Identifiers: chr16:g.68867231T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68833328T>C , CM000678.2:g.68833328T>C	GRCh38
NC_000016.9:g.68867231T>C , CM000678.1:g.68867231T>C	GRCh37
NC_000016.8:g.67424732T>C	NCBI36
NG_008021.1:g.101037T>C , LRG_301:g.101037T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2478T>C MANE Select	ENSP00000261769.4:p.Pro826=
ENST00000261769.9:c.2478T>C	ENSP00000261769.4:p.Pro826=
ENST00000422392.6:c.2295T>C	ENSP00000414946.2:p.Pro765=
ENST00000562118.1:n.696T>C
ENST00000562836.5:n.2549T>C
ENST00000566510.5:c.*1144T>C	ENSP00000458139.1:n.*1144T>C
ENST00000566612.5:c.*718T>C	ENSP00000454782.1:n.*718T>C
ENST00000611625.4:c.2541T>C	ENSP00000481063.1:p.Pro847=
ENST00000612417.4:c.1854-863T>C	ENSP00000478360.1:n.1854-863T>C
ENST00000621016.4:c.1866-875T>C	ENSP00000480664.1:n.1866-875T>C
NM_004360.3:c.2478T>C , LRG_301t1:c.2478T>C	NP_004351.1:p.Pro826=
XM_011523488.1:c.1743T>C	XP_011521790.1:p.Pro581=
XM_011523489.1:c.1743T>C	XP_011521791.1:p.Pro581=
NM_001317184.1:c.2295T>C	NP_001304113.1:p.Pro765=
NM_001317185.1:c.930T>C	NP_001304114.1:p.Pro310=
NM_001317186.1:c.513T>C	NP_001304115.1:p.Pro171=
NM_004360.4:c.2478T>C	NP_004351.1:p.Pro826=
NM_004360.5:c.2478T>C MANE Select	NP_004351.1:p.Pro826=
NM_001317184.2:c.2295T>C	NP_001304113.1:p.Pro765=
NM_001317185.2:c.930T>C	NP_001304114.1:p.Pro310=
NM_001317186.2:c.513T>C	NP_001304115.1:p.Pro171=