Canonical Allele Identifier: CA396462812

Gene: CDH1

Linked Data

• MyVariant Identifiers: chr16:g.68849469A>G (hg19) ; chr16:g.68815566A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68815566A>G , CM000678.2:g.68815566A>G	GRCh38
NC_000016.9:g.68849469A>G , CM000678.1:g.68849469A>G	GRCh37
NC_000016.8:g.67406970A>G	NCBI36
NG_008021.1:g.83275A>G , LRG_301:g.83275A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1372A>G MANE Select	ENSP00000261769.4:p.Asn458Asp
ENST00000261769.9:c.1372A>G	ENSP00000261769.4:p.Asn458Asp
ENST00000422392.6:c.1189A>G	ENSP00000414946.2:p.Asn397Asp
ENST00000562836.5:n.1443A>G
ENST00000566510.5:c.*38A>G	ENSP00000458139.1:n.*38A>G
ENST00000566612.5:c.1372A>G	ENSP00000454782.1:p.Asn458Asp
ENST00000611625.4:c.1435A>G	ENSP00000481063.1:p.Asn479Asp
ENST00000612417.4:c.1372A>G	ENSP00000478360.1:p.Asn458Asp
ENST00000621016.4:c.1372A>G	ENSP00000480664.1:p.Asn458Asp
NM_004360.3:c.1372A>G , LRG_301t1:c.1372A>G	NP_004351.1:p.Asn458Asp
XM_011523488.1:c.637A>G	XP_011521790.1:p.Asn213Asp
XM_011523489.1:c.637A>G	XP_011521791.1:p.Asn213Asp
NM_001317184.1:c.1189A>G	NP_001304113.1:p.Asn397Asp
NM_001317185.1:c.-177A>G	NP_001304114.1:n.-177A>G
NM_001317186.1:c.-448A>G	NP_001304115.1:n.-448A>G
NM_004360.4:c.1372A>G	NP_004351.1:p.Asn458Asp
NM_004360.5:c.1372A>G MANE Select	NP_004351.1:p.Asn458Asp
NM_001317184.2:c.1189A>G	NP_001304113.1:p.Asn397Asp
NM_001317185.2:c.-177A>G	NP_001304114.1:n.-177A>G
NM_001317186.2:c.-448A>G	NP_001304115.1:n.-448A>G