Canonical Allele Identifier: CA2208645073
Community Standard Title: NM_001145204.3(SHISA9):c.692-58354T>G
Gene: SHISA9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13145040T>G , CM000678.2:g.13145040T>G GRCh38
NC_000016.9:g.13238897T>G , CM000678.1:g.13238897T>G GRCh37
NC_000016.8:g.13146398T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001145204.3:c.692-58354T>G MANE Select NP_001138676.2:n.692-58354T>G
ENST00000558583.3:c.692-58354T>G MANE Select ENSP00000454014.2:n.692-58354T>G
NM_001145204.2:c.692-58354T>G NP_001138676.2:n.692-58354T>G
ENST00000558583.2:c.692-58354T>G ENSP00000454014.2:n.692-58354T>G
ENST00000566106.1:n.136-58354T>G
XM_005255539.2:c.815-58354T>G XP_005255596.2:n.815-58354T>G
XM_005255539.3:c.815-58354T>G XP_005255596.2:n.815-58354T>G
XM_011522642.1:c.815-58354T>G XP_011520944.1:n.815-58354T>G
XM_011522642.2:c.815-58354T>G XP_011520944.1:n.815-58354T>G
XM_011522643.1:c.815-58354T>G XP_011520945.1:n.815-58354T>G
XR_001751976.1:n.1138-58354T>G
XR_932915.1:n.1115-58354T>G
XR_932915.2:n.1138-58354T>G