Canonical Allele Identifier: CA396467198

Gene: CDH1

Linked Data

• dbSNP Id: rs2152138566
• MyVariant Identifiers: chr16:g.68856096G>A (hg19) ; chr16:g.68822193G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822193G>A , CM000678.2:g.68822193G>A	GRCh38
NC_000016.9:g.68856096G>A , CM000678.1:g.68856096G>A	GRCh37
NC_000016.8:g.67413597G>A	NCBI36
NG_008021.1:g.89902G>A , LRG_301:g.89902G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.1904G>A MANE Select	ENSP00000261769.4:p.Ser635Asn
ENST00000261769.9:c.1904G>A	ENSP00000261769.4:p.Ser635Asn
ENST00000422392.6:c.1721G>A	ENSP00000414946.2:p.Ser574Asn
ENST00000562836.5:n.1975G>A
ENST00000566510.5:c.*570G>A	ENSP00000458139.1:n.*570G>A
ENST00000566612.5:c.*144G>A	ENSP00000454782.1:n.*144G>A
ENST00000611625.4:c.1967G>A	ENSP00000481063.1:p.Ser656Asn
ENST00000612417.4:c.1830+74G>A	ENSP00000478360.1:n.1830+74G>A
ENST00000621016.4:c.1865+39G>A	ENSP00000480664.1:n.1865+39G>A
NM_004360.3:c.1904G>A , LRG_301t1:c.1904G>A	NP_004351.1:p.Ser635Asn
XM_011523488.1:c.1169G>A	XP_011521790.1:p.Ser390Asn
XM_011523489.1:c.1169G>A	XP_011521791.1:p.Ser390Asn
NM_001317184.1:c.1721G>A	NP_001304113.1:p.Ser574Asn
NM_001317185.1:c.356G>A	NP_001304114.1:p.Ser119Asn
NM_001317186.1:c.-62G>A	NP_001304115.1:n.-62G>A
NM_004360.4:c.1904G>A	NP_004351.1:p.Ser635Asn
NM_004360.5:c.1904G>A MANE Select	NP_004351.1:p.Ser635Asn
NM_001317184.2:c.1721G>A	NP_001304113.1:p.Ser574Asn
NM_001317185.2:c.356G>A	NP_001304114.1:p.Ser119Asn
NM_001317186.2:c.-62G>A	NP_001304115.1:n.-62G>A