Canonical Allele Identifier: CA1534797747
Gene: CDH9 HGNC NCBI

Linked Data

dbSNP Id: rs1741374823

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.26927982T>C , CM000667.2:g.26927982T>C GRCh38
NC_000005.9:g.26928090T>C , CM000667.1:g.26928090T>C GRCh37
NC_000005.8:g.26963847T>C NCBI36
NG_046968.1:g.198217A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000231021.9:c.229-12058A>G MANE Select ENSP00000231021.4:n.229-12058A>G
ENST00000231021.8:c.229-12058A>G ENSP00000231021.4:n.229-12058A>G
ENST00000505045.1:n.402-12058A>G
ENST00000511822.1:c.229-12058A>G ENSP00000422538.1:n.229-12058A>G
ENST00000513289.5:c.229-12058A>G ENSP00000426239.1:n.229-12058A>G
NM_016279.3:c.229-12058A>G NP_057363.3:n.229-12058A>G
XM_011513922.1:c.229-12058A>G XP_011512224.1:n.229-12058A>G
NM_016279.4:c.229-12058A>G MANE Select NP_057363.3:n.229-12058A>G