Canonical Allele Identifier: CA2708255081
Gene: CDH9 HGNC NCBI

Linked Data

dbSNP Id: rs200686923

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.26928082_26928084dup , CM000667.2:g.26928082_26928084dup GRCh38
NC_000005.9:g.26928190_26928192dup , CM000667.1:g.26928190_26928192dup GRCh37
NC_000005.8:g.26963947_26963949dup NCBI36
NG_046968.1:g.198118_198120dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000231021.9:c.229-12157_229-12155dup MANE Select ENSP00000231021.4:n.229-12157_229-12155dup
ENST00000231021.8:c.229-12157_229-12155dup ENSP00000231021.4:n.229-12157_229-12155dup
ENST00000505045.1:n.402-12157_402-12155dup
ENST00000511822.1:c.229-12157_229-12155dup ENSP00000422538.1:n.229-12157_229-12155dup
ENST00000513289.5:c.229-12157_229-12155dup ENSP00000426239.1:n.229-12157_229-12155dup
NM_016279.3:c.229-12157_229-12155dup NP_057363.3:n.229-12157_229-12155dup
XM_011513922.1:c.229-12157_229-12155dup XP_011512224.1:n.229-12157_229-12155dup
NM_016279.4:c.229-12157_229-12155dup MANE Select NP_057363.3:n.229-12157_229-12155dup