Canonical Allele Identifier: CA375098636

Gene: SPTAN1

Linked Data

• MyVariant Identifiers: chr9:g.131394547C>A (hg19) ; chr9:g.128632268C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128632268C>A , CM000671.2:g.128632268C>A	GRCh38
NC_000009.11:g.131394547C>A , CM000671.1:g.131394547C>A	GRCh37
NC_000009.10:g.130434368C>A	NCBI36
NG_027748.1:g.84711C>A
NG_034056.1:g.29583G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627441.3:c.6940C>A	ENSP00000486547.2:p.Leu2314Met
ENST00000630866.2:c.6967C>A	ENSP00000487444.1:p.Leu2323Met
ENST00000704202.1:c.6991C>A	ENSP00000515764.1:p.Leu2331Met
ENST00000704203.1:c.6940C>A	ENSP00000515765.1:p.Leu2314Met
ENST00000704204.1:c.6430C>A	ENSP00000515766.1:p.Leu2144Met
ENST00000704206.1:c.4509C>A
ENST00000704207.1:c.2846C>A
ENST00000706487.1:c.6904C>A	ENSP00000516412.1:p.Leu2302Met
ENST00000372739.7:c.6904C>A MANE Select	ENSP00000361824.4:p.Leu2302Met
ENST00000636010.1:n.628C>A
ENST00000358161.9:c.6829C>A	ENSP00000350882.6:p.Leu2277Met
ENST00000372731.8:c.6889C>A	ENSP00000361816.4:p.Leu2297Met
ENST00000372739.5:c.6904C>A	ENSP00000361824.3:p.Leu2302Met
ENST00000625980.2:n.858C>A
ENST00000630763.1:n.661C>A
ENST00000630804.2:c.6844C>A	ENSP00000486308.1:p.Leu2282Met
ENST00000630866.1:c.6967C>A	ENSP00000487444.1:p.Leu2323Met
NM_001130438.2:c.6904C>A	NP_001123910.1:p.Leu2302Met
NM_001195532.1:c.6829C>A	NP_001182461.1:p.Leu2277Met
NM_003127.3:c.6889C>A	NP_003118.2:p.Leu2297Met
XM_006717245.1:c.7003C>A	XP_006717308.1:p.Leu2335Met
XM_006717246.1:c.6988C>A	XP_006717309.1:p.Leu2330Met
XM_006717247.1:c.6943C>A	XP_006717310.1:p.Leu2315Met
XM_006717248.1:c.6940C>A	XP_006717311.1:p.Leu2314Met
XM_006717249.1:c.6925C>A	XP_006717312.1:p.Leu2309Met
XM_006717250.1:c.6922C>A	XP_006717313.1:p.Leu2308Met
XM_006717251.1:c.6907C>A	XP_006717314.1:p.Leu2303Met
XM_006717252.1:c.6880C>A	XP_006717315.1:p.Leu2294Met
XM_006717253.1:c.6865C>A	XP_006717316.1:p.Leu2289Met
XM_006717254.1:c.6967C>A	XP_006717317.1:p.Leu2323Met
NM_001363759.1:c.6967C>A	NP_001350688.1:p.Leu2323Met
NM_001363765.1:c.6844C>A	NP_001350694.1:p.Leu2282Met
XM_006717247.2:c.6943C>A	XP_006717310.1:p.Leu2315Met
XM_006717248.2:c.6940C>A	XP_006717311.1:p.Leu2314Met
XM_006717251.2:c.6907C>A	XP_006717314.1:p.Leu2303Met
XM_006717252.3:c.6880C>A	XP_006717315.1:p.Leu2294Met
XM_017015059.1:c.6886C>A	XP_016870548.1:p.Leu2296Met
XM_017015060.1:c.6862C>A	XP_016870549.1:p.Leu2288Met
NM_001130438.3:c.6904C>A MANE Select	NP_001123910.1:p.Leu2302Met
NM_001195532.2:c.6829C>A	NP_001182461.1:p.Leu2277Met
NM_001363759.2:c.6967C>A	NP_001350688.1:p.Leu2323Met
NM_001363765.2:c.6844C>A	NP_001350694.1:p.Leu2282Met
NM_001375310.1:c.6991C>A	NP_001362239.1:p.Leu2331Met
NM_001375311.2:c.6904C>A	NP_001362240.1:p.Leu2302Met
NM_001375312.2:c.6940C>A	NP_001362241.2:p.Leu2314Met
NM_001375313.1:c.6886C>A	NP_001362242.1:p.Leu2296Met
NM_001375314.2:c.6844C>A	NP_001362243.1:p.Leu2282Met
NM_001375318.1:c.7003C>A	NP_001362247.1:p.Leu2335Met
NM_003127.4:c.6889C>A	NP_003118.2:p.Leu2297Met