Canonical Allele Identifier: CA718146363

Gene: SHISA9

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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