Canonical Allele Identifier: CA2229980303
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68822027A= , CM000678.2:g.68822027A= GRCh38
NC_000016.9:g.68855930A= , CM000678.1:g.68855930A= GRCh37
NC_000016.8:g.67413431A= NCBI36
NG_008021.1:g.89736A= , LRG_301:g.89736A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.1738A= MANE Select ENSP00000261769.4:p.Thr580=
ENST00000261769.9:c.1738A= ENSP00000261769.4:p.Thr580=
ENST00000422392.6:c.1555A= ENSP00000414946.2:p.Thr519=
ENST00000562836.5:n.1809A=
ENST00000566510.5:c.*404A= ENSP00000458139.1:n.*404A=
ENST00000566612.5:c.1592A= ENSP00000454782.1:p.Asp531=
ENST00000611625.4:c.1801A= ENSP00000481063.1:p.Thr601=
ENST00000612417.4:c.1738A= ENSP00000478360.1:p.Thr580=
ENST00000621016.4:c.1738A= ENSP00000480664.1:p.Thr580=
NM_004360.3:c.1738A= , LRG_301t1:c.1738A= NP_004351.1:p.Thr580=
XM_011523488.1:c.1003A= XP_011521790.1:p.Thr335=
XM_011523489.1:c.1003A= XP_011521791.1:p.Thr335=
NM_001317184.1:c.1555A= NP_001304113.1:p.Thr519=
NM_001317185.1:c.190A= NP_001304114.1:p.Thr64=
NM_001317186.1:c.-228A= NP_001304115.1:n.-228A=
NM_004360.4:c.1738A= NP_004351.1:p.Thr580=
NM_004360.5:c.1738A= MANE Select NP_004351.1:p.Thr580=
NM_001317184.2:c.1555A= NP_001304113.1:p.Thr519=
NM_001317185.2:c.190A= NP_001304114.1:p.Thr64=
NM_001317186.2:c.-228A= NP_001304115.1:n.-228A=