Canonical Allele Identifier: CA1534797800

Gene: CDH9

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.26928062_26928063delinsAT , CM000667.2:g.26928062_26928063delinsAT	GRCh38
NC_000005.9:g.26928170_26928171delinsAT , CM000667.1:g.26928170_26928171delinsAT	GRCh37
NC_000005.8:g.26963927_26963928delinsAT	NCBI36
NG_046968.1:g.198136_198137delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231021.9:c.229-12139_229-12138delinsAT MANE Select	ENSP00000231021.4:n.229-12139_229-12138delinsAT
ENST00000231021.8:c.229-12139_229-12138delinsAT	ENSP00000231021.4:n.229-12139_229-12138delinsAT
ENST00000505045.1:n.402-12139_402-12138delinsAT
ENST00000511822.1:c.229-12139_229-12138delinsAT	ENSP00000422538.1:n.229-12139_229-12138delinsAT
ENST00000513289.5:c.229-12139_229-12138delinsAT	ENSP00000426239.1:n.229-12139_229-12138delinsAT
NM_016279.3:c.229-12139_229-12138delinsAT	NP_057363.3:n.229-12139_229-12138delinsAT
XM_011513922.1:c.229-12139_229-12138delinsAT	XP_011512224.1:n.229-12139_229-12138delinsAT
NM_016279.4:c.229-12139_229-12138delinsAT MANE Select	NP_057363.3:n.229-12139_229-12138delinsAT