Canonical Allele Identifier: CA396466789

Gene: CDH1

Linked Data

• MyVariant Identifiers: chr16:g.68856005A>T (hg19) ; chr16:g.68822102A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822102A>T , CM000678.2:g.68822102A>T	GRCh38
NC_000016.9:g.68856005A>T , CM000678.1:g.68856005A>T	GRCh37
NC_000016.8:g.67413506A>T	NCBI36
NG_008021.1:g.89811A>T , LRG_301:g.89811A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1813A>T MANE Select	ENSP00000261769.4:p.Arg605Trp
ENST00000261769.9:c.1813A>T	ENSP00000261769.4:p.Arg605Trp
ENST00000422392.6:c.1630A>T	ENSP00000414946.2:p.Arg544Trp
ENST00000562836.5:n.1884A>T
ENST00000566510.5:c.*479A>T	ENSP00000458139.1:n.*479A>T
ENST00000566612.5:c.*53A>T	ENSP00000454782.1:n.*53A>T
ENST00000611625.4:c.1876A>T	ENSP00000481063.1:p.Arg626Trp
ENST00000612417.4:c.1813A>T	ENSP00000478360.1:p.Arg605Trp
ENST00000621016.4:c.1813A>T	ENSP00000480664.1:p.Arg605Trp
NM_004360.3:c.1813A>T , LRG_301t1:c.1813A>T	NP_004351.1:p.Arg605Trp
XM_011523488.1:c.1078A>T	XP_011521790.1:p.Arg360Trp
XM_011523489.1:c.1078A>T	XP_011521791.1:p.Arg360Trp
NM_001317184.1:c.1630A>T	NP_001304113.1:p.Arg544Trp
NM_001317185.1:c.265A>T	NP_001304114.1:p.Arg89Trp
NM_001317186.1:c.-153A>T	NP_001304115.1:n.-153A>T
NM_004360.4:c.1813A>T	NP_004351.1:p.Arg605Trp
NM_004360.5:c.1813A>T MANE Select	NP_004351.1:p.Arg605Trp
NM_001317184.2:c.1630A>T	NP_001304113.1:p.Arg544Trp
NM_001317185.2:c.265A>T	NP_001304114.1:p.Arg89Trp
NM_001317186.2:c.-153A>T	NP_001304115.1:n.-153A>T