Canonical Allele Identifier: CA809324247

Gene: CDH9

Linked Data

• dbSNP Id: rs1196928378
• gnomAD v3: 5-26928043-CTTAAG-C
• gnomAD v4: 5-26928043-CTTAAG-C
• MyVariant Identifiers: chr5:g.26928152_26928156del (hg19) ; chr5:g.26928044_26928048del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.26928048_26928052del , CM000667.2:g.26928048_26928052del	GRCh38
NC_000005.9:g.26928156_26928160del , CM000667.1:g.26928156_26928160del	GRCh37
NC_000005.8:g.26963913_26963917del	NCBI36
NG_046968.1:g.198151_198155del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231021.9:c.229-12124_229-12120del MANE Select	ENSP00000231021.4:n.229-12124_229-12120del
ENST00000231021.8:c.229-12124_229-12120del	ENSP00000231021.4:n.229-12124_229-12120del
ENST00000505045.1:n.402-12124_402-12120del
ENST00000511822.1:c.229-12124_229-12120del	ENSP00000422538.1:n.229-12124_229-12120del
ENST00000513289.5:c.229-12124_229-12120del	ENSP00000426239.1:n.229-12124_229-12120del
NM_016279.3:c.229-12124_229-12120del	NP_057363.3:n.229-12124_229-12120del
XM_011513922.1:c.229-12124_229-12120del	XP_011512224.1:n.229-12124_229-12120del
NM_016279.4:c.229-12124_229-12120del MANE Select	NP_057363.3:n.229-12124_229-12120del