Canonical Allele Identifier: CA396467601

Gene: CDH1

Linked Data

• MyVariant Identifiers: chr16:g.68857350A>C (hg19) ; chr16:g.68823447A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68823447A>C , CM000678.2:g.68823447A>C	GRCh38
NC_000016.9:g.68857350A>C , CM000678.1:g.68857350A>C	GRCh37
NC_000016.8:g.67414851A>C	NCBI36
NG_008021.1:g.91156A>C , LRG_301:g.91156A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1985A>C MANE Select	ENSP00000261769.4:p.Asp662Ala
ENST00000261769.9:c.1985A>C	ENSP00000261769.4:p.Asp662Ala
ENST00000422392.6:c.1802A>C	ENSP00000414946.2:p.Asp601Ala
ENST00000562118.1:n.203A>C
ENST00000562836.5:n.2056A>C
ENST00000566510.5:c.*651A>C	ENSP00000458139.1:n.*651A>C
ENST00000566612.5:c.*225A>C	ENSP00000454782.1:n.*225A>C
ENST00000611625.4:c.2048A>C	ENSP00000481063.1:p.Asp683Ala
ENST00000612417.4:c.1830+1328A>C	ENSP00000478360.1:n.1830+1328A>C
ENST00000621016.4:c.1865+1293A>C	ENSP00000480664.1:n.1865+1293A>C
NM_004360.3:c.1985A>C , LRG_301t1:c.1985A>C	NP_004351.1:p.Asp662Ala
XM_011523488.1:c.1250A>C	XP_011521790.1:p.Asp417Ala
XM_011523489.1:c.1250A>C	XP_011521791.1:p.Asp417Ala
NM_001317184.1:c.1802A>C	NP_001304113.1:p.Asp601Ala
NM_001317185.1:c.437A>C	NP_001304114.1:p.Asp146Ala
NM_001317186.1:c.20A>C	NP_001304115.1:p.Asp7Ala
NM_004360.4:c.1985A>C	NP_004351.1:p.Asp662Ala
NM_004360.5:c.1985A>C MANE Select	NP_004351.1:p.Asp662Ala
NM_001317184.2:c.1802A>C	NP_001304113.1:p.Asp601Ala
NM_001317185.2:c.437A>C	NP_001304114.1:p.Asp146Ala
NM_001317186.2:c.20A>C	NP_001304115.1:p.Asp7Ala