Canonical Allele Identifier: CA396457148

Gene: CDH1

Linked Data

• dbSNP Id: rs1060501247
• MyVariant Identifiers: chr16:g.68835608G>C (hg19) ; chr16:g.68801705G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68801705G>C , CM000678.2:g.68801705G>C	GRCh38
NC_000016.9:g.68835608G>C , CM000678.1:g.68835608G>C	GRCh37
NC_000016.8:g.67393109G>C	NCBI36
NG_008021.1:g.69414G>C , LRG_301:g.69414G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.199G>C MANE Select	ENSP00000261769.4:p.Ala67Pro
ENST00000261769.9:c.199G>C	ENSP00000261769.4:p.Ala67Pro
ENST00000422392.6:c.199G>C	ENSP00000414946.2:p.Ala67Pro
ENST00000562836.5:n.270G>C
ENST00000564676.5:n.481G>C
ENST00000564745.1:n.194G>C
ENST00000566510.5:c.199G>C	ENSP00000458139.1:p.Ala67Pro
ENST00000566612.5:c.199G>C	ENSP00000454782.1:p.Ala67Pro
ENST00000611625.4:c.199G>C	ENSP00000481063.1:p.Ala67Pro
ENST00000612417.4:c.199G>C	ENSP00000478360.1:p.Ala67Pro
ENST00000621016.4:c.199G>C	ENSP00000480664.1:p.Ala67Pro
NM_004360.3:c.199G>C , LRG_301t1:c.199G>C	NP_004351.1:p.Ala67Pro
XM_011523488.1:c.-537G>C	XP_011521790.1:n.-537G>C
XM_011523489.1:c.-537G>C	XP_011521791.1:n.-537G>C
NM_001317184.1:c.199G>C	NP_001304113.1:p.Ala67Pro
NM_001317185.1:c.-1417G>C	NP_001304114.1:n.-1417G>C
NM_001317186.1:c.-1621G>C	NP_001304115.1:n.-1621G>C
NM_004360.4:c.199G>C	NP_004351.1:p.Ala67Pro
NM_004360.5:c.199G>C MANE Select	NP_004351.1:p.Ala67Pro
NM_001317184.2:c.199G>C	NP_001304113.1:p.Ala67Pro
NM_001317185.2:c.-1417G>C	NP_001304114.1:n.-1417G>C
NM_001317186.2:c.-1621G>C	NP_001304115.1:n.-1621G>C