Canonical Allele Identifier: CA1074375840
Gene: CDH9 HGNC NCBI

Linked Data

dbSNP Id: rs1741374066

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.26927959del , CM000667.2:g.26927959del GRCh38
NC_000005.9:g.26928067del , CM000667.1:g.26928067del GRCh37
NC_000005.8:g.26963824del NCBI36
NG_046968.1:g.198241del

Transcript Alleles

HGVS Amino-acid change
ENST00000231021.9:c.229-12034del MANE Select ENSP00000231021.4:n.229-12034del
ENST00000231021.8:c.229-12034del ENSP00000231021.4:n.229-12034del
ENST00000505045.1:n.402-12034del
ENST00000511822.1:c.229-12034del ENSP00000422538.1:n.229-12034del
ENST00000513289.5:c.229-12034del ENSP00000426239.1:n.229-12034del
NM_016279.3:c.229-12034del NP_057363.3:n.229-12034del
XM_011513922.1:c.229-12034del XP_011512224.1:n.229-12034del
NM_016279.4:c.229-12034del MANE Select NP_057363.3:n.229-12034del