Canonical Allele Identifier: CA396451249
Community Standard Title: NM_004360.5(CDH1):c.12G>A (p.Trp4Ter)
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68737427G>A , CM000678.2:g.68737427G>A GRCh38
NC_000016.9:g.68771330G>A , CM000678.1:g.68771330G>A GRCh37
NC_000016.8:g.67328831G>A NCBI36
NG_008021.1:g.5136G>A , LRG_301:g.5136G>A

Transcript Alleles

HGVS Amino-acid Change
NM_004360.5:c.12G>A MANE Select NP_004351.1:p.Trp4Ter
ENST00000261769.10:c.12G>A MANE Select ENSP00000261769.4:p.Trp4Ter
NM_001317184.1:c.12G>A NP_001304113.1:p.Trp4Ter
NM_001317184.2:c.12G>A NP_001304113.1:p.Trp4Ter
NM_001317185.1:c.-1604G>A NP_001304114.1:n.-1604G>A
NM_001317185.2:c.-1604G>A NP_001304114.1:n.-1604G>A
NM_001317186.1:c.-1808G>A NP_001304115.1:n.-1808G>A
NM_001317186.2:c.-1808G>A NP_001304115.1:n.-1808G>A
NM_004360.3:c.12G>A , LRG_301t1:c.12G>A NP_004351.1:p.Trp4Ter
NM_004360.4:c.12G>A NP_004351.1:p.Trp4Ter
ENST00000261769.9:c.12G>A ENSP00000261769.4:p.Trp4Ter
ENST00000422392.6:c.12G>A ENSP00000414946.2:p.Trp4Ter
ENST00000566510.5:c.12G>A ENSP00000458139.1:p.Trp4Ter
ENST00000566612.5:c.12G>A ENSP00000454782.1:p.Trp4Ter
ENST00000611625.4:c.12G>A ENSP00000481063.1:p.Trp4Ter
ENST00000612417.4:c.12G>A ENSP00000478360.1:p.Trp4Ter
ENST00000621016.4:c.12G>A ENSP00000480664.1:p.Trp4Ter