Canonical Allele Identifier: CA2229992054
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829672C= , CM000678.2:g.68829672C= GRCh38
NC_000016.9:g.68863575C= , CM000678.1:g.68863575C= GRCh37
NC_000016.8:g.67421076C= NCBI36
NG_008021.1:g.97381C= , LRG_301:g.97381C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2314C= MANE Select ENSP00000261769.4:p.Leu772=
ENST00000261769.9:c.2314C= ENSP00000261769.4:p.Leu772=
ENST00000422392.6:c.2131C= ENSP00000414946.2:p.Leu711=
ENST00000562118.1:n.532C=
ENST00000562836.5:n.2385C=
ENST00000566510.5:c.*980C= ENSP00000458139.1:n.*980C=
ENST00000566612.5:c.*554C= ENSP00000454782.1:n.*554C=
ENST00000611625.4:c.2377C= ENSP00000481063.1:p.Leu793=
ENST00000612417.4:c.1853+3118C= ENSP00000478360.1:n.1853+3118C=
ENST00000621016.4:c.1866-4531C= ENSP00000480664.1:n.1866-4531C=
NM_004360.3:c.2314C= , LRG_301t1:c.2314C= NP_004351.1:p.Leu772=
XM_011523488.1:c.1579C= XP_011521790.1:p.Leu527=
XM_011523489.1:c.1579C= XP_011521791.1:p.Leu527=
NM_001317184.1:c.2131C= NP_001304113.1:p.Leu711=
NM_001317185.1:c.766C= NP_001304114.1:p.Leu256=
NM_001317186.1:c.349C= NP_001304115.1:p.Leu117=
NM_004360.4:c.2314C= NP_004351.1:p.Leu772=
NM_004360.5:c.2314C= MANE Select NP_004351.1:p.Leu772=
NM_001317184.2:c.2131C= NP_001304113.1:p.Leu711=
NM_001317185.2:c.766C= NP_001304114.1:p.Leu256=
NM_001317186.2:c.349C= NP_001304115.1:p.Leu117=