Canonical Allele Identifier: CA396467050

Gene: CDH1

Linked Data

• dbSNP Id: rs2152138474
• MyVariant Identifiers: chr16:g.68856054C>T (hg19) ; chr16:g.68822151C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822151C>T , CM000678.2:g.68822151C>T	GRCh38
NC_000016.9:g.68856054C>T , CM000678.1:g.68856054C>T	GRCh37
NC_000016.8:g.67413555C>T	NCBI36
NG_008021.1:g.89860C>T , LRG_301:g.89860C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1862C>T MANE Select	ENSP00000261769.4:p.Pro621Leu
ENST00000261769.9:c.1862C>T	ENSP00000261769.4:p.Pro621Leu
ENST00000422392.6:c.1679C>T	ENSP00000414946.2:p.Pro560Leu
ENST00000562836.5:n.1933C>T
ENST00000566510.5:c.*528C>T	ENSP00000458139.1:n.*528C>T
ENST00000566612.5:c.*102C>T	ENSP00000454782.1:n.*102C>T
ENST00000611625.4:c.1925C>T	ENSP00000481063.1:p.Pro642Leu
ENST00000612417.4:c.1830+32C>T	ENSP00000478360.1:n.1830+32C>T
ENST00000621016.4:c.1862C>T	ENSP00000480664.1:p.Pro621Leu
NM_004360.3:c.1862C>T , LRG_301t1:c.1862C>T	NP_004351.1:p.Pro621Leu
XM_011523488.1:c.1127C>T	XP_011521790.1:p.Pro376Leu
XM_011523489.1:c.1127C>T	XP_011521791.1:p.Pro376Leu
NM_001317184.1:c.1679C>T	NP_001304113.1:p.Pro560Leu
NM_001317185.1:c.314C>T	NP_001304114.1:p.Pro105Leu
NM_001317186.1:c.-104C>T	NP_001304115.1:n.-104C>T
NM_004360.4:c.1862C>T	NP_004351.1:p.Pro621Leu
NM_004360.5:c.1862C>T MANE Select	NP_004351.1:p.Pro621Leu
NM_001317184.2:c.1679C>T	NP_001304113.1:p.Pro560Leu
NM_001317185.2:c.314C>T	NP_001304114.1:p.Pro105Leu
NM_001317186.2:c.-104C>T	NP_001304115.1:n.-104C>T