Canonical Allele Identifier: CA375097909

Gene: SPTAN1

Linked Data

• MyVariant Identifiers: chr9:g.131394488T>G (hg19) ; chr9:g.128632209T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128632209T>G , CM000671.2:g.128632209T>G	GRCh38
NC_000009.11:g.131394488T>G , CM000671.1:g.131394488T>G	GRCh37
NC_000009.10:g.130434309T>G	NCBI36
NG_027748.1:g.84652T>G
NG_034056.1:g.29642A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627441.3:c.6881T>G	ENSP00000486547.2:p.Ile2294Ser
ENST00000630866.2:c.6908T>G	ENSP00000487444.1:p.Ile2303Ser
ENST00000704202.1:c.6932T>G	ENSP00000515764.1:p.Ile2311Ser
ENST00000704203.1:c.6881T>G	ENSP00000515765.1:p.Ile2294Ser
ENST00000704204.1:c.6371T>G	ENSP00000515766.1:p.Ile2124Ser
ENST00000704206.1:c.4450T>G
ENST00000704207.1:c.2787T>G
ENST00000706487.1:c.6845T>G	ENSP00000516412.1:p.Ile2282Ser
ENST00000372739.7:c.6845T>G MANE Select	ENSP00000361824.4:p.Ile2282Ser
ENST00000636010.1:n.569T>G
ENST00000358161.9:c.6770T>G	ENSP00000350882.6:p.Ile2257Ser
ENST00000372731.8:c.6830T>G	ENSP00000361816.4:p.Ile2277Ser
ENST00000372739.5:c.6845T>G	ENSP00000361824.3:p.Ile2282Ser
ENST00000625980.2:n.799T>G
ENST00000630763.1:n.602T>G
ENST00000630804.2:c.6785T>G	ENSP00000486308.1:p.Ile2262Ser
ENST00000630866.1:c.6908T>G	ENSP00000487444.1:p.Ile2303Ser
NM_001130438.2:c.6845T>G	NP_001123910.1:p.Ile2282Ser
NM_001195532.1:c.6770T>G	NP_001182461.1:p.Ile2257Ser
NM_003127.3:c.6830T>G	NP_003118.2:p.Ile2277Ser
XM_006717245.1:c.6944T>G	XP_006717308.1:p.Ile2315Ser
XM_006717246.1:c.6929T>G	XP_006717309.1:p.Ile2310Ser
XM_006717247.1:c.6884T>G	XP_006717310.1:p.Ile2295Ser
XM_006717248.1:c.6881T>G	XP_006717311.1:p.Ile2294Ser
XM_006717249.1:c.6866T>G	XP_006717312.1:p.Ile2289Ser
XM_006717250.1:c.6863T>G	XP_006717313.1:p.Ile2288Ser
XM_006717251.1:c.6848T>G	XP_006717314.1:p.Ile2283Ser
XM_006717252.1:c.6821T>G	XP_006717315.1:p.Ile2274Ser
XM_006717253.1:c.6806T>G	XP_006717316.1:p.Ile2269Ser
XM_006717254.1:c.6908T>G	XP_006717317.1:p.Ile2303Ser
NM_001363759.1:c.6908T>G	NP_001350688.1:p.Ile2303Ser
NM_001363765.1:c.6785T>G	NP_001350694.1:p.Ile2262Ser
XM_006717247.2:c.6884T>G	XP_006717310.1:p.Ile2295Ser
XM_006717248.2:c.6881T>G	XP_006717311.1:p.Ile2294Ser
XM_006717251.2:c.6848T>G	XP_006717314.1:p.Ile2283Ser
XM_006717252.3:c.6821T>G	XP_006717315.1:p.Ile2274Ser
XM_017015059.1:c.6827T>G	XP_016870548.1:p.Ile2276Ser
XM_017015060.1:c.6803T>G	XP_016870549.1:p.Ile2268Ser
NM_001130438.3:c.6845T>G MANE Select	NP_001123910.1:p.Ile2282Ser
NM_001195532.2:c.6770T>G	NP_001182461.1:p.Ile2257Ser
NM_001363759.2:c.6908T>G	NP_001350688.1:p.Ile2303Ser
NM_001363765.2:c.6785T>G	NP_001350694.1:p.Ile2262Ser
NM_001375310.1:c.6932T>G	NP_001362239.1:p.Ile2311Ser
NM_001375311.2:c.6845T>G	NP_001362240.1:p.Ile2282Ser
NM_001375312.2:c.6881T>G	NP_001362241.2:p.Ile2294Ser
NM_001375313.1:c.6827T>G	NP_001362242.1:p.Ile2276Ser
NM_001375314.2:c.6785T>G	NP_001362243.1:p.Ile2262Ser
NM_001375318.1:c.6944T>G	NP_001362247.1:p.Ile2315Ser
NM_003127.4:c.6830T>G	NP_003118.2:p.Ile2277Ser