Canonical Allele Identifier: CA375097768

Gene: SPTAN1

Linked Data

• MyVariant Identifiers: chr9:g.131394476A>G (hg19) ; chr9:g.128632197A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128632197A>G , CM000671.2:g.128632197A>G	GRCh38
NC_000009.11:g.131394476A>G , CM000671.1:g.131394476A>G	GRCh37
NC_000009.10:g.130434297A>G	NCBI36
NG_027748.1:g.84640A>G
NG_034056.1:g.29654T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627441.3:c.6869A>G	ENSP00000486547.2:p.Glu2290Gly
ENST00000630866.2:c.6896A>G	ENSP00000487444.1:p.Glu2299Gly
ENST00000704202.1:c.6920A>G	ENSP00000515764.1:p.Glu2307Gly
ENST00000704203.1:c.6869A>G	ENSP00000515765.1:p.Glu2290Gly
ENST00000704204.1:c.6359A>G	ENSP00000515766.1:p.Glu2120Gly
ENST00000704206.1:c.4438A>G
ENST00000704207.1:c.2775A>G
ENST00000706487.1:c.6833A>G	ENSP00000516412.1:p.Glu2278Gly
ENST00000372739.7:c.6833A>G MANE Select	ENSP00000361824.4:p.Glu2278Gly
ENST00000636010.1:n.557A>G
ENST00000358161.9:c.6758A>G	ENSP00000350882.6:p.Glu2253Gly
ENST00000372731.8:c.6818A>G	ENSP00000361816.4:p.Glu2273Gly
ENST00000372739.5:c.6833A>G	ENSP00000361824.3:p.Glu2278Gly
ENST00000625980.2:n.787A>G
ENST00000630763.1:n.590A>G
ENST00000630804.2:c.6773A>G	ENSP00000486308.1:p.Glu2258Gly
ENST00000630866.1:c.6896A>G	ENSP00000487444.1:p.Glu2299Gly
NM_001130438.2:c.6833A>G	NP_001123910.1:p.Glu2278Gly
NM_001195532.1:c.6758A>G	NP_001182461.1:p.Glu2253Gly
NM_003127.3:c.6818A>G	NP_003118.2:p.Glu2273Gly
XM_006717245.1:c.6932A>G	XP_006717308.1:p.Glu2311Gly
XM_006717246.1:c.6917A>G	XP_006717309.1:p.Glu2306Gly
XM_006717247.1:c.6872A>G	XP_006717310.1:p.Glu2291Gly
XM_006717248.1:c.6869A>G	XP_006717311.1:p.Glu2290Gly
XM_006717249.1:c.6854A>G	XP_006717312.1:p.Glu2285Gly
XM_006717250.1:c.6851A>G	XP_006717313.1:p.Glu2284Gly
XM_006717251.1:c.6836A>G	XP_006717314.1:p.Glu2279Gly
XM_006717252.1:c.6809A>G	XP_006717315.1:p.Glu2270Gly
XM_006717253.1:c.6794A>G	XP_006717316.1:p.Glu2265Gly
XM_006717254.1:c.6896A>G	XP_006717317.1:p.Glu2299Gly
NM_001363759.1:c.6896A>G	NP_001350688.1:p.Glu2299Gly
NM_001363765.1:c.6773A>G	NP_001350694.1:p.Glu2258Gly
XM_006717247.2:c.6872A>G	XP_006717310.1:p.Glu2291Gly
XM_006717248.2:c.6869A>G	XP_006717311.1:p.Glu2290Gly
XM_006717251.2:c.6836A>G	XP_006717314.1:p.Glu2279Gly
XM_006717252.3:c.6809A>G	XP_006717315.1:p.Glu2270Gly
XM_017015059.1:c.6815A>G	XP_016870548.1:p.Glu2272Gly
XM_017015060.1:c.6791A>G	XP_016870549.1:p.Glu2264Gly
NM_001130438.3:c.6833A>G MANE Select	NP_001123910.1:p.Glu2278Gly
NM_001195532.2:c.6758A>G	NP_001182461.1:p.Glu2253Gly
NM_001363759.2:c.6896A>G	NP_001350688.1:p.Glu2299Gly
NM_001363765.2:c.6773A>G	NP_001350694.1:p.Glu2258Gly
NM_001375310.1:c.6920A>G	NP_001362239.1:p.Glu2307Gly
NM_001375311.2:c.6833A>G	NP_001362240.1:p.Glu2278Gly
NM_001375312.2:c.6869A>G	NP_001362241.2:p.Glu2290Gly
NM_001375313.1:c.6815A>G	NP_001362242.1:p.Glu2272Gly
NM_001375314.2:c.6773A>G	NP_001362243.1:p.Glu2258Gly
NM_001375318.1:c.6932A>G	NP_001362247.1:p.Glu2311Gly
NM_003127.4:c.6818A>G	NP_003118.2:p.Glu2273Gly