Canonical Allele Identifier: CA1534797728
Gene: CDH9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.26927961_26927962delinsTG , CM000667.2:g.26927961_26927962delinsTG GRCh38
NC_000005.9:g.26928069_26928070delinsTG , CM000667.1:g.26928069_26928070delinsTG GRCh37
NC_000005.8:g.26963826_26963827delinsTG NCBI36
NG_046968.1:g.198237_198238delinsCA

Transcript Alleles

HGVS Amino-acid change
ENST00000231021.9:c.229-12038_229-12037delinsCA MANE Select ENSP00000231021.4:n.229-12038_229-12037de...
ENST00000231021.8:c.229-12038_229-12037delinsCA ENSP00000231021.4:n.229-12038_229-12037de...
ENST00000505045.1:n.402-12038_402-12037delinsCA
ENST00000511822.1:c.229-12038_229-12037delinsCA ENSP00000422538.1:n.229-12038_229-12037de...
ENST00000513289.5:c.229-12038_229-12037delinsCA ENSP00000426239.1:n.229-12038_229-12037de...
NM_016279.3:c.229-12038_229-12037delinsCA NP_057363.3:n.229-12038_229-12037delinsCA...
XM_011513922.1:c.229-12038_229-12037delinsCA XP_011512224.1:n.229-12038_229-12037delin...
NM_016279.4:c.229-12038_229-12037delinsCA MANE Select NP_057363.3:n.229-12038_229-12037delinsCA...