Canonical Allele Identifier: CA1074375835
Gene: CDH9 HGNC NCBI

Linked Data

dbSNP Id: rs1741372479
gnomAD v3: 5-26927894-G-A
gnomAD v4: 5-26927894-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.26927894G>A , CM000667.2:g.26927894G>A GRCh38
NC_000005.9:g.26928002G>A , CM000667.1:g.26928002G>A GRCh37
NC_000005.8:g.26963759G>A NCBI36
NG_046968.1:g.198305C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000231021.9:c.229-11970C>T MANE Select ENSP00000231021.4:n.229-11970C>T
ENST00000231021.8:c.229-11970C>T ENSP00000231021.4:n.229-11970C>T
ENST00000505045.1:n.402-11970C>T
ENST00000511822.1:c.229-11970C>T ENSP00000422538.1:n.229-11970C>T
ENST00000513289.5:c.229-11970C>T ENSP00000426239.1:n.229-11970C>T
NM_016279.3:c.229-11970C>T NP_057363.3:n.229-11970C>T
XM_011513922.1:c.229-11970C>T XP_011512224.1:n.229-11970C>T
NM_016279.4:c.229-11970C>T MANE Select NP_057363.3:n.229-11970C>T