Canonical Allele Identifier: CA2229991700
Gene: CDH1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829523T= , CM000678.2:g.68829523T= GRCh38
NC_000016.9:g.68863426T= , CM000678.1:g.68863426T= GRCh37
NC_000016.8:g.67420927T= NCBI36
NG_008021.1:g.97232T= , LRG_301:g.97232T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2296-131T= MANE Select ENSP00000261769.4:n.2296-131T=
ENST00000261769.9:c.2296-131T= ENSP00000261769.4:n.2296-131T=
ENST00000422392.6:c.2113-131T= ENSP00000414946.2:n.2113-131T=
ENST00000562118.1:n.514-131T=
ENST00000562836.5:n.2367-131T=
ENST00000566510.5:c.*962-131T= ENSP00000458139.1:n.*962-131T=
ENST00000566612.5:c.*536-131T= ENSP00000454782.1:n.*536-131T=
ENST00000611625.4:c.2359-131T= ENSP00000481063.1:n.2359-131T=
ENST00000612417.4:c.1853+2969T= ENSP00000478360.1:n.1853+2969T=
ENST00000621016.4:c.1866-4680T= ENSP00000480664.1:n.1866-4680T=
NM_004360.3:c.2296-131T= , LRG_301t1:c.2296-131T= NP_004351.1:n.2296-131T=
XM_011523488.1:c.1561-131T= XP_011521790.1:n.1561-131T=
XM_011523489.1:c.1561-131T= XP_011521791.1:n.1561-131T=
NM_001317184.1:c.2113-131T= NP_001304113.1:n.2113-131T=
NM_001317185.1:c.748-131T= NP_001304114.1:n.748-131T=
NM_001317186.1:c.331-131T= NP_001304115.1:n.331-131T=
NM_004360.4:c.2296-131T= NP_004351.1:n.2296-131T=
NM_004360.5:c.2296-131T= MANE Select NP_004351.1:n.2296-131T=
NM_001317184.2:c.2113-131T= NP_001304113.1:n.2113-131T=
NM_001317185.2:c.748-131T= NP_001304114.1:n.748-131T=
NM_001317186.2:c.331-131T= NP_001304115.1:n.331-131T=
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