Canonical Allele Identifier: CA15917830

Gene: SPIRE1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.12606464G>T , CM000680.2:g.12606464G>T	GRCh38
NC_000018.9:g.12606463G>T , CM000680.1:g.12606463G>T	GRCh37
NC_000018.8:g.12596463G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409402.9:c.372+28598C>A MANE Select	ENSP00000387266.3:n.372+28598C>A
ENST00000309836.9:c.12+28598C>A	ENSP00000309661.5:n.12+28598C>A
ENST00000409402.8:c.372+28598C>A	ENSP00000387266.3:n.372+28598C>A
ENST00000410092.7:c.372+28598C>A	ENSP00000387226.3:n.372+28598C>A
ENST00000440472.6:c.-149-18045C>A	ENSP00000404752.1:n.-149-18045C>A
ENST00000449797.5:c.12+28598C>A	ENSP00000401392.1:n.12+28598C>A
ENST00000453447.6:c.12+28598C>A	ENSP00000407050.1:n.12+28598C>A
ENST00000462226.1:c.12+28598C>A	ENSP00000467943.1:n.12+28598C>A
ENST00000497844.6:c.66+28598C>A	ENSP00000467103.1:n.66+28598C>A
NM_001128626.1:c.372+28598C>A	NP_001122098.1:n.372+28598C>A
NM_001128627.1:c.12+28598C>A	NP_001122099.1:n.12+28598C>A
NM_020148.2:c.372+28598C>A	NP_064533.3:n.372+28598C>A
XM_005258122.3:c.372+28598C>A	XP_005258179.1:n.372+28598C>A
XM_011525700.1:c.372+28598C>A	XP_011524002.1:n.372+28598C>A
XM_011525701.1:c.372+28598C>A	XP_011524003.1:n.372+28598C>A
XM_011525702.1:c.12+28598C>A	XP_011524004.1:n.12+28598C>A
XM_011525703.1:c.372+28598C>A	XP_011524005.1:n.372+28598C>A
XM_005258122.4:c.372+28598C>A	XP_005258179.1:n.372+28598C>A
XM_011525703.2:c.372+28598C>A	XP_011524005.1:n.372+28598C>A
XM_024451224.1:c.12+28598C>A	XP_024306992.1:n.12+28598C>A
XM_024451225.1:c.48+28598C>A	XP_024306993.1:n.48+28598C>A
NM_001128626.2:c.372+28598C>A MANE Select	NP_001122098.1:n.372+28598C>A
NM_020148.3:c.372+28598C>A	NP_064533.3:n.372+28598C>A
NM_001394323.1:c.48+28598C>A	NP_001381252.1:n.48+28598C>A
NM_001394324.1:c.12+28598C>A	NP_001381253.1:n.12+28598C>A
NM_001394325.1:c.-149-18045C>A	NP_001381254.1:n.-149-18045C>A