Canonical Allele Identifier: CA1534797671
Gene: CDH9 HGNC NCBI

Linked Data

dbSNP Id: rs1741371971

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.26927875C>G , CM000667.2:g.26927875C>G GRCh38
NC_000005.9:g.26927983C>G , CM000667.1:g.26927983C>G GRCh37
NC_000005.8:g.26963740C>G NCBI36
NG_046968.1:g.198324G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000231021.9:c.229-11951G>C MANE Select ENSP00000231021.4:n.229-11951G>C
ENST00000231021.8:c.229-11951G>C ENSP00000231021.4:n.229-11951G>C
ENST00000505045.1:n.402-11951G>C
ENST00000511822.1:c.229-11951G>C ENSP00000422538.1:n.229-11951G>C
ENST00000513289.5:c.229-11951G>C ENSP00000426239.1:n.229-11951G>C
NM_016279.3:c.229-11951G>C NP_057363.3:n.229-11951G>C
XM_011513922.1:c.229-11951G>C XP_011512224.1:n.229-11951G>C
NM_016279.4:c.229-11951G>C MANE Select NP_057363.3:n.229-11951G>C