Canonical Allele Identifier: CA1534797598

Gene: CDH9

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.26927750_26927752delinsAAG , CM000667.2:g.26927750_26927752delinsAAG	GRCh38
NC_000005.9:g.26927858_26927860delinsAAG , CM000667.1:g.26927858_26927860delinsAAG	GRCh37
NC_000005.8:g.26963615_26963617delinsAAG	NCBI36
NG_046968.1:g.198447_198449delinsCTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000231021.9:c.229-11828_229-11826delinsCTT MANE Select	ENSP00000231021.4:n.229-11828_229-11826delinsCTT
ENST00000231021.8:c.229-11828_229-11826delinsCTT	ENSP00000231021.4:n.229-11828_229-11826delinsCTT
ENST00000505045.1:n.402-11828_402-11826delinsCTT
ENST00000511822.1:c.229-11828_229-11826delinsCTT	ENSP00000422538.1:n.229-11828_229-11826delinsCTT
ENST00000513289.5:c.229-11828_229-11826delinsCTT	ENSP00000426239.1:n.229-11828_229-11826delinsCTT
NM_016279.3:c.229-11828_229-11826delinsCTT	NP_057363.3:n.229-11828_229-11826delinsCTT
XM_011513922.1:c.229-11828_229-11826delinsCTT	XP_011512224.1:n.229-11828_229-11826delinsCTT
NM_016279.4:c.229-11828_229-11826delinsCTT MANE Select	NP_057363.3:n.229-11828_229-11826delinsCTT