Canonical Allele Identifier: CA396472822

Gene: CDH1

Linked Data

• dbSNP Id: rs1555518291
• MyVariant Identifiers: chr16:g.68867378G>C (hg19) ; chr16:g.68833475G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68833475G>C , CM000678.2:g.68833475G>C	GRCh38
NC_000016.9:g.68867378G>C , CM000678.1:g.68867378G>C	GRCh37
NC_000016.8:g.67424879G>C	NCBI36
NG_008021.1:g.101184G>C , LRG_301:g.101184G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2625G>C MANE Select	ENSP00000261769.4:p.Met875Ile
ENST00000261769.9:c.2625G>C	ENSP00000261769.4:p.Met875Ile
ENST00000422392.6:c.2442G>C	ENSP00000414946.2:p.Met814Ile
ENST00000562118.1:n.843G>C
ENST00000562836.5:n.2696G>C
ENST00000566510.5:c.*1291G>C	ENSP00000458139.1:n.*1291G>C
ENST00000566612.5:c.*865G>C	ENSP00000454782.1:n.*865G>C
ENST00000611625.4:c.2688G>C	ENSP00000481063.1:p.Met896Ile
ENST00000612417.4:c.1854-716G>C	ENSP00000478360.1:n.1854-716G>C
ENST00000621016.4:c.1866-728G>C	ENSP00000480664.1:n.1866-728G>C
NM_004360.3:c.2625G>C , LRG_301t1:c.2625G>C	NP_004351.1:p.Met875Ile
XM_011523488.1:c.1890G>C	XP_011521790.1:p.Met630Ile
XM_011523489.1:c.1890G>C	XP_011521791.1:p.Met630Ile
NM_001317184.1:c.2442G>C	NP_001304113.1:p.Met814Ile
NM_001317185.1:c.1077G>C	NP_001304114.1:p.Met359Ile
NM_001317186.1:c.660G>C	NP_001304115.1:p.Met220Ile
NM_004360.4:c.2625G>C	NP_004351.1:p.Met875Ile
NM_004360.5:c.2625G>C MANE Select	NP_004351.1:p.Met875Ile
NM_001317184.2:c.2442G>C	NP_001304113.1:p.Met814Ile
NM_001317185.2:c.1077G>C	NP_001304114.1:p.Met359Ile
NM_001317186.2:c.660G>C	NP_001304115.1:p.Met220Ile