Canonical Allele Identifier: CA115746527
Gene: CDH9 HGNC NCBI

Linked Data

dbSNP Id: rs909529419
gnomAD v3: 5-26927975-A-T
gnomAD v4: 5-26927975-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.26927975A>T , CM000667.2:g.26927975A>T GRCh38
NC_000005.9:g.26928083A>T , CM000667.1:g.26928083A>T GRCh37
NC_000005.8:g.26963840A>T NCBI36
NG_046968.1:g.198224T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000231021.9:c.229-12051T>A MANE Select ENSP00000231021.4:n.229-12051T>A
ENST00000231021.8:c.229-12051T>A ENSP00000231021.4:n.229-12051T>A
ENST00000505045.1:n.402-12051T>A
ENST00000511822.1:c.229-12051T>A ENSP00000422538.1:n.229-12051T>A
ENST00000513289.5:c.229-12051T>A ENSP00000426239.1:n.229-12051T>A
NM_016279.3:c.229-12051T>A NP_057363.3:n.229-12051T>A
XM_011513922.1:c.229-12051T>A XP_011512224.1:n.229-12051T>A
NM_016279.4:c.229-12051T>A MANE Select NP_057363.3:n.229-12051T>A