Canonical Allele Identifier: CA1534797788

Gene: CDH9

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.26928043_26928048delinsCTTAAG , CM000667.2:g.26928043_26928048delinsCTTAAG	GRCh38
NC_000005.9:g.26928151_26928156delinsCTTAAG , CM000667.1:g.26928151_26928156delinsCTTAAG	GRCh37
NC_000005.8:g.26963908_26963913delinsCTTAAG	NCBI36
NG_046968.1:g.198151_198156delinsCTTAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231021.9:c.229-12124_229-12119delinsCTTAAG MANE Select	ENSP00000231021.4:n.229-12124_229-12119delinsCTTAAG
ENST00000231021.8:c.229-12124_229-12119delinsCTTAAG	ENSP00000231021.4:n.229-12124_229-12119delinsCTTAAG
ENST00000505045.1:n.402-12124_402-12119delinsCTTAAG
ENST00000511822.1:c.229-12124_229-12119delinsCTTAAG	ENSP00000422538.1:n.229-12124_229-12119delinsCTTAAG
ENST00000513289.5:c.229-12124_229-12119delinsCTTAAG	ENSP00000426239.1:n.229-12124_229-12119delinsCTTAAG
NM_016279.3:c.229-12124_229-12119delinsCTTAAG	NP_057363.3:n.229-12124_229-12119delinsCTTAAG
XM_011513922.1:c.229-12124_229-12119delinsCTTAAG	XP_011512224.1:n.229-12124_229-12119delinsCTTAAG
NM_016279.4:c.229-12124_229-12119delinsCTTAAG MANE Select	NP_057363.3:n.229-12124_229-12119delinsCTTAAG