Canonical Allele Identifier: CA2566216290
Gene: CDH9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.26927707_26927708insTT , CM000667.2:g.26927707_26927708insTT GRCh38
NC_000005.9:g.26927815_26927816insTT , CM000667.1:g.26927815_26927816insTT GRCh37
NC_000005.8:g.26963572_26963573insTT NCBI36
NG_046968.1:g.198491_198492insAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000231021.9:c.229-11784_229-11783insAA MANE Select ENSP00000231021.4:n.229-11784_229-11783insAA
ENST00000231021.8:c.229-11784_229-11783insAA ENSP00000231021.4:n.229-11784_229-11783insAA
ENST00000505045.1:n.402-11784_402-11783insAA
ENST00000511822.1:c.229-11784_229-11783insAA ENSP00000422538.1:n.229-11784_229-11783insAA
ENST00000513289.5:c.229-11784_229-11783insAA ENSP00000426239.1:n.229-11784_229-11783insAA
NM_016279.3:c.229-11784_229-11783insAA NP_057363.3:n.229-11784_229-11783insAA
XM_011513922.1:c.229-11784_229-11783insAA XP_011512224.1:n.229-11784_229-11783insAA
NM_016279.4:c.229-11784_229-11783insAA MANE Select NP_057363.3:n.229-11784_229-11783insAA
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