Canonical Allele Identifier: CA115746307
Gene: CDH9 HGNC NCBI

Linked Data

dbSNP Id: rs956069286
MyVariant Identifiers: chr5:g.26927854C>T (hg19) chr5:g.26927746C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.26927746C>T , CM000667.2:g.26927746C>T GRCh38
NC_000005.9:g.26927854C>T , CM000667.1:g.26927854C>T GRCh37
NC_000005.8:g.26963611C>T NCBI36
NG_046968.1:g.198453G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000231021.9:c.229-11822G>A MANE Select ENSP00000231021.4:n.229-11822G>A
ENST00000231021.8:c.229-11822G>A ENSP00000231021.4:n.229-11822G>A
ENST00000505045.1:n.402-11822G>A
ENST00000511822.1:c.229-11822G>A ENSP00000422538.1:n.229-11822G>A
ENST00000513289.5:c.229-11822G>A ENSP00000426239.1:n.229-11822G>A
NM_016279.3:c.229-11822G>A NP_057363.3:n.229-11822G>A
XM_011513922.1:c.229-11822G>A XP_011512224.1:n.229-11822G>A
NM_016279.4:c.229-11822G>A MANE Select NP_057363.3:n.229-11822G>A
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