Canonical Allele Identifier: CA115746287

Gene: CDH9

Linked Data

• dbSNP Id: rs558201176
• gnomAD v3: 5-26927693-C-T
• gnomAD v4: 5-26927693-C-T
• MyVariant Identifiers: chr5:g.26927801C>T (hg19) ; chr5:g.26927693C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.26927693C>T , CM000667.2:g.26927693C>T	GRCh38
NC_000005.9:g.26927801C>T , CM000667.1:g.26927801C>T	GRCh37
NC_000005.8:g.26963558C>T	NCBI36
NG_046968.1:g.198506G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231021.9:c.229-11769G>A MANE Select	ENSP00000231021.4:n.229-11769G>A
ENST00000231021.8:c.229-11769G>A	ENSP00000231021.4:n.229-11769G>A
ENST00000505045.1:n.402-11769G>A
ENST00000511822.1:c.229-11769G>A	ENSP00000422538.1:n.229-11769G>A
ENST00000513289.5:c.229-11769G>A	ENSP00000426239.1:n.229-11769G>A
NM_016279.3:c.229-11769G>A	NP_057363.3:n.229-11769G>A
XM_011513922.1:c.229-11769G>A	XP_011512224.1:n.229-11769G>A
NM_016279.4:c.229-11769G>A MANE Select	NP_057363.3:n.229-11769G>A