Canonical Allele Identifier: CA1534797806
Gene: CDH9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.26928078_26928081delinsATCT , CM000667.2:g.26928078_26928081delinsATCT GRCh38
NC_000005.9:g.26928186_26928189delinsATCT , CM000667.1:g.26928186_26928189delinsATCT GRCh37
NC_000005.8:g.26963943_26963946delinsATCT NCBI36
NG_046968.1:g.198118_198121delinsAGAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000231021.9:c.229-12157_229-12154delinsAGAT MANE Select ENSP00000231021.4:n.229-12157_229-12154delinsAGAT
ENST00000231021.8:c.229-12157_229-12154delinsAGAT ENSP00000231021.4:n.229-12157_229-12154delinsAGAT
ENST00000505045.1:n.402-12157_402-12154delinsAGAT
ENST00000511822.1:c.229-12157_229-12154delinsAGAT ENSP00000422538.1:n.229-12157_229-12154delinsAGAT
ENST00000513289.5:c.229-12157_229-12154delinsAGAT ENSP00000426239.1:n.229-12157_229-12154delinsAGAT
NM_016279.3:c.229-12157_229-12154delinsAGAT NP_057363.3:n.229-12157_229-12154delinsAGAT
XM_011513922.1:c.229-12157_229-12154delinsAGAT XP_011512224.1:n.229-12157_229-12154delinsAGAT
NM_016279.4:c.229-12157_229-12154delinsAGAT MANE Select NP_057363.3:n.229-12157_229-12154delinsAGAT