Canonical Allele Identifier: CA1074375854
Gene: CDH9 HGNC NCBI

Linked Data

dbSNP Id: rs1741378138
gnomAD v3: 5-26928127-T-G
gnomAD v4: 5-26928127-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.26928127T>G , CM000667.2:g.26928127T>G GRCh38
NC_000005.9:g.26928235T>G , CM000667.1:g.26928235T>G GRCh37
NC_000005.8:g.26963992T>G NCBI36
NG_046968.1:g.198072A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000231021.9:c.229-12203A>C MANE Select ENSP00000231021.4:n.229-12203A>C
ENST00000231021.8:c.229-12203A>C ENSP00000231021.4:n.229-12203A>C
ENST00000505045.1:n.402-12203A>C
ENST00000511822.1:c.229-12203A>C ENSP00000422538.1:n.229-12203A>C
ENST00000513289.5:c.229-12203A>C ENSP00000426239.1:n.229-12203A>C
NM_016279.3:c.229-12203A>C NP_057363.3:n.229-12203A>C
XM_011513922.1:c.229-12203A>C XP_011512224.1:n.229-12203A>C
NM_016279.4:c.229-12203A>C MANE Select NP_057363.3:n.229-12203A>C
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