Canonical Allele Identifier: CA2208645071

Gene: SHISA9

Genomic Alleles

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

Transcript Alleles

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