Canonical Allele Identifier: CA278812141

Gene: SHISA9

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13160099G>T , CM000678.2:g.13160099G>T	GRCh38
NC_000016.9:g.13253956G>T , CM000678.1:g.13253956G>T	GRCh37
NC_000016.8:g.13161457G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558583.3:c.692-43295G>T MANE Select	ENSP00000454014.2:n.692-43295G>T
ENST00000558583.2:c.692-43295G>T	ENSP00000454014.2:n.692-43295G>T
ENST00000566106.1:n.136-43295G>T
NM_001145204.2:c.692-43295G>T	NP_001138676.2:n.692-43295G>T
XM_005255539.2:c.815-43295G>T	XP_005255596.2:n.815-43295G>T
XM_011522642.1:c.815-43295G>T	XP_011520944.1:n.815-43295G>T
XM_011522643.1:c.815-43295G>T	XP_011520945.1:n.815-43295G>T
XR_932915.1:n.1115-43295G>T
XM_005255539.3:c.815-43295G>T	XP_005255596.2:n.815-43295G>T
XM_011522642.2:c.815-43295G>T	XP_011520944.1:n.815-43295G>T
XR_001751976.1:n.1138-43295G>T
XR_932915.2:n.1138-43295G>T
NM_001145204.3:c.692-43295G>T MANE Select	NP_001138676.2:n.692-43295G>T