Canonical Allele Identifier: CA2208545690

Gene: SHISA9

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.12967754T= , CM000678.2:g.12967754T=	GRCh38
NC_000016.9:g.13061611T= , CM000678.1:g.13061611T=	GRCh37
NC_000016.8:g.12969112T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558583.3:c.691+50939T= MANE Select	ENSP00000454014.2:n.691+50939T=
ENST00000558583.2:c.691+50939T=	ENSP00000454014.2:n.691+50939T=
NM_001145204.2:c.691+50939T=	NP_001138676.2:n.691+50939T=
XM_005255539.2:c.814+50939T=	XP_005255596.2:n.814+50939T=
XM_011522642.1:c.814+50939T=	XP_011520944.1:n.814+50939T=
XM_011522643.1:c.814+50939T=	XP_011520945.1:n.814+50939T=
XR_932915.1:n.1114+50939T=
XM_005255539.3:c.814+50939T=	XP_005255596.2:n.814+50939T=
XM_011522642.2:c.814+50939T=	XP_011520944.1:n.814+50939T=
XR_001751976.1:n.1137+50939T=
XR_932915.2:n.1137+50939T=
NM_001145204.3:c.691+50939T= MANE Select	NP_001138676.2:n.691+50939T=