Canonical Allele Identifier: CA2590240573
Gene: SPIRE1 HGNC NCBI

Linked Data

dbSNP Id: rs2144065362

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.12516771C>T , CM000680.2:g.12516771C>T GRCh38
NC_000018.9:g.12516770C>T , CM000680.1:g.12516770C>T GRCh37
NC_000018.8:g.12506770C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000409402.9:c.730-4240G>A MANE Select ENSP00000387266.3:n.730-4240G>A
ENST00000309836.9:c.139-4240G>A ENSP00000309661.5:n.139-4240G>A
ENST00000409402.8:c.730-4240G>A ENSP00000387266.3:n.730-4240G>A
ENST00000410092.7:c.730-4240G>A ENSP00000387226.3:n.730-4240G>A
ENST00000440472.6:c.253-4240G>A ENSP00000404752.1:n.253-4240G>A
ENST00000449797.5:c.370-4240G>A ENSP00000401392.1:n.370-4240G>A
ENST00000453447.6:c.370-4240G>A ENSP00000407050.1:n.370-4240G>A
ENST00000497844.6:c.424-4240G>A ENSP00000467103.1:n.424-4240G>A
ENST00000626255.2:c.370-4240G>A ENSP00000486927.1:n.370-4240G>A
NM_001128626.1:c.730-4240G>A NP_001122098.1:n.730-4240G>A
NM_001128627.1:c.370-4240G>A NP_001122099.1:n.370-4240G>A
NM_020148.2:c.730-4240G>A NP_064533.3:n.730-4240G>A
XM_005258122.3:c.730-4240G>A XP_005258179.1:n.730-4240G>A
XM_011525700.1:c.730-4240G>A XP_011524002.1:n.730-4240G>A
XM_011525701.1:c.730-4240G>A XP_011524003.1:n.730-4240G>A
XM_011525702.1:c.370-4240G>A XP_011524004.1:n.370-4240G>A
XM_011525703.1:c.730-4240G>A XP_011524005.1:n.730-4240G>A
XM_005258122.4:c.730-4240G>A XP_005258179.1:n.730-4240G>A
XM_011525703.2:c.730-4240G>A XP_011524005.1:n.730-4240G>A
XM_024451224.1:c.370-4240G>A XP_024306992.1:n.370-4240G>A
XM_024451225.1:c.406-4240G>A XP_024306993.1:n.406-4240G>A
NM_001128626.2:c.730-4240G>A MANE Select NP_001122098.1:n.730-4240G>A
NM_020148.3:c.730-4240G>A NP_064533.3:n.730-4240G>A
NM_001394323.1:c.406-4240G>A NP_001381252.1:n.406-4240G>A
NM_001394324.1:c.139-4240G>A NP_001381253.1:n.139-4240G>A
NM_001394325.1:c.253-4240G>A NP_001381254.1:n.253-4240G>A