Canonical Allele Identifier: CA809323995
Gene: CDH9 HGNC NCBI

Linked Data

dbSNP Id: rs1213714292
MyVariant Identifiers: chr5:g.26927922_26927923insT (hg19) chr5:g.26927814_26927815insT (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.26927815dup , CM000667.2:g.26927815dup GRCh38
NC_000005.9:g.26927923dup , CM000667.1:g.26927923dup GRCh37
NC_000005.8:g.26963680dup NCBI36
NG_046968.1:g.198384dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000231021.9:c.229-11891dup MANE Select ENSP00000231021.4:n.229-11891dup
ENST00000231021.8:c.229-11891dup ENSP00000231021.4:n.229-11891dup
ENST00000505045.1:n.402-11891dup
ENST00000511822.1:c.229-11891dup ENSP00000422538.1:n.229-11891dup
ENST00000513289.5:c.229-11891dup ENSP00000426239.1:n.229-11891dup
NM_016279.3:c.229-11891dup NP_057363.3:n.229-11891dup
XM_011513922.1:c.229-11891dup XP_011512224.1:n.229-11891dup
NM_016279.4:c.229-11891dup MANE Select NP_057363.3:n.229-11891dup
Search 100 bp 5'
Search 100 bp 3'