Canonical Allele Identifier: CA1534797677
Gene: CDH9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.26927885G= , CM000667.2:g.26927885G= GRCh38
NC_000005.9:g.26927993G= , CM000667.1:g.26927993G= GRCh37
NC_000005.8:g.26963750G= NCBI36
NG_046968.1:g.198314C=

Transcript Alleles

HGVS Amino-acid change
ENST00000231021.9:c.229-11961C= MANE Select ENSP00000231021.4:n.229-11961C=
ENST00000231021.8:c.229-11961C= ENSP00000231021.4:n.229-11961C=
ENST00000505045.1:n.402-11961C=
ENST00000511822.1:c.229-11961C= ENSP00000422538.1:n.229-11961C=
ENST00000513289.5:c.229-11961C= ENSP00000426239.1:n.229-11961C=
NM_016279.3:c.229-11961C= NP_057363.3:n.229-11961C=
XM_011513922.1:c.229-11961C= XP_011512224.1:n.229-11961C=
NM_016279.4:c.229-11961C= MANE Select NP_057363.3:n.229-11961C=