Canonical Allele Identifier: CA1534797732
Gene: CDH9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.26927965A= , CM000667.2:g.26927965A= GRCh38
NC_000005.9:g.26928073A= , CM000667.1:g.26928073A= GRCh37
NC_000005.8:g.26963830A= NCBI36
NG_046968.1:g.198234T=

Transcript Alleles

HGVS Amino-acid change
ENST00000231021.9:c.229-12041T= MANE Select ENSP00000231021.4:n.229-12041T=
ENST00000231021.8:c.229-12041T= ENSP00000231021.4:n.229-12041T=
ENST00000505045.1:n.402-12041T=
ENST00000511822.1:c.229-12041T= ENSP00000422538.1:n.229-12041T=
ENST00000513289.5:c.229-12041T= ENSP00000426239.1:n.229-12041T=
NM_016279.3:c.229-12041T= NP_057363.3:n.229-12041T=
XM_011513922.1:c.229-12041T= XP_011512224.1:n.229-12041T=
NM_016279.4:c.229-12041T= MANE Select NP_057363.3:n.229-12041T=