Canonical Allele Identifier: CA558436651

Gene: CDH9

Linked Data

• dbSNP Id: rs1330778149
• gnomAD v2: 5-26928032-A-G
• gnomAD v3: 5-26927924-A-G
• gnomAD v4: 5-26927924-A-G
• MyVariant Identifiers: chr5:g.26928032A>G (hg19) ; chr5:g.26927924A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.26927924A>G , CM000667.2:g.26927924A>G	GRCh38
NC_000005.9:g.26928032A>G , CM000667.1:g.26928032A>G	GRCh37
NC_000005.8:g.26963789A>G	NCBI36
NG_046968.1:g.198275T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231021.9:c.229-12000T>C MANE Select	ENSP00000231021.4:n.229-12000T>C
ENST00000231021.8:c.229-12000T>C	ENSP00000231021.4:n.229-12000T>C
ENST00000505045.1:n.402-12000T>C
ENST00000511822.1:c.229-12000T>C	ENSP00000422538.1:n.229-12000T>C
ENST00000513289.5:c.229-12000T>C	ENSP00000426239.1:n.229-12000T>C
NM_016279.3:c.229-12000T>C	NP_057363.3:n.229-12000T>C
XM_011513922.1:c.229-12000T>C	XP_011512224.1:n.229-12000T>C
NM_016279.4:c.229-12000T>C MANE Select	NP_057363.3:n.229-12000T>C