Canonical Allele Identifier: CA375098949

Gene: SPTAN1

Linked Data

• MyVariant Identifiers: chr9:g.131394578A>T (hg19) ; chr9:g.128632299A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128632299A>T , CM000671.2:g.128632299A>T	GRCh38
NC_000009.11:g.131394578A>T , CM000671.1:g.131394578A>T	GRCh37
NC_000009.10:g.130434399A>T	NCBI36
NG_027748.1:g.84742A>T
NG_034056.1:g.29552T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627441.3:c.6971A>T	ENSP00000486547.2:p.Asn2324Ile
ENST00000630866.2:c.6998A>T	ENSP00000487444.1:p.Asn2333Ile
ENST00000704202.1:c.7022A>T	ENSP00000515764.1:p.Asn2341Ile
ENST00000704203.1:c.6971A>T	ENSP00000515765.1:p.Asn2324Ile
ENST00000704204.1:c.6461A>T	ENSP00000515766.1:p.Asn2154Ile
ENST00000704206.1:c.4540A>T
ENST00000704207.1:c.2877A>T
ENST00000706487.1:c.6935A>T	ENSP00000516412.1:p.Asn2312Ile
ENST00000372739.7:c.6935A>T MANE Select	ENSP00000361824.4:p.Asn2312Ile
ENST00000636010.1:n.659A>T
ENST00000358161.9:c.6860A>T	ENSP00000350882.6:p.Asn2287Ile
ENST00000372731.8:c.6920A>T	ENSP00000361816.4:p.Asn2307Ile
ENST00000372739.5:c.6935A>T	ENSP00000361824.3:p.Asn2312Ile
ENST00000625980.2:n.889A>T
ENST00000630763.1:n.692A>T
ENST00000630804.2:c.6875A>T	ENSP00000486308.1:p.Asn2292Ile
ENST00000630866.1:c.6998A>T	ENSP00000487444.1:p.Asn2333Ile
NM_001130438.2:c.6935A>T	NP_001123910.1:p.Asn2312Ile
NM_001195532.1:c.6860A>T	NP_001182461.1:p.Asn2287Ile
NM_003127.3:c.6920A>T	NP_003118.2:p.Asn2307Ile
XM_006717245.1:c.7034A>T	XP_006717308.1:p.Asn2345Ile
XM_006717246.1:c.7019A>T	XP_006717309.1:p.Asn2340Ile
XM_006717247.1:c.6974A>T	XP_006717310.1:p.Asn2325Ile
XM_006717248.1:c.6971A>T	XP_006717311.1:p.Asn2324Ile
XM_006717249.1:c.6956A>T	XP_006717312.1:p.Asn2319Ile
XM_006717250.1:c.6953A>T	XP_006717313.1:p.Asn2318Ile
XM_006717251.1:c.6938A>T	XP_006717314.1:p.Asn2313Ile
XM_006717252.1:c.6911A>T	XP_006717315.1:p.Asn2304Ile
XM_006717253.1:c.6896A>T	XP_006717316.1:p.Asn2299Ile
XM_006717254.1:c.6998A>T	XP_006717317.1:p.Asn2333Ile
NM_001363759.1:c.6998A>T	NP_001350688.1:p.Asn2333Ile
NM_001363765.1:c.6875A>T	NP_001350694.1:p.Asn2292Ile
XM_006717247.2:c.6974A>T	XP_006717310.1:p.Asn2325Ile
XM_006717248.2:c.6971A>T	XP_006717311.1:p.Asn2324Ile
XM_006717251.2:c.6938A>T	XP_006717314.1:p.Asn2313Ile
XM_006717252.3:c.6911A>T	XP_006717315.1:p.Asn2304Ile
XM_017015059.1:c.6917A>T	XP_016870548.1:p.Asn2306Ile
XM_017015060.1:c.6893A>T	XP_016870549.1:p.Asn2298Ile
NM_001130438.3:c.6935A>T MANE Select	NP_001123910.1:p.Asn2312Ile
NM_001195532.2:c.6860A>T	NP_001182461.1:p.Asn2287Ile
NM_001363759.2:c.6998A>T	NP_001350688.1:p.Asn2333Ile
NM_001363765.2:c.6875A>T	NP_001350694.1:p.Asn2292Ile
NM_001375310.1:c.7022A>T	NP_001362239.1:p.Asn2341Ile
NM_001375311.2:c.6935A>T	NP_001362240.1:p.Asn2312Ile
NM_001375312.2:c.6971A>T	NP_001362241.2:p.Asn2324Ile
NM_001375313.1:c.6917A>T	NP_001362242.1:p.Asn2306Ile
NM_001375314.2:c.6875A>T	NP_001362243.1:p.Asn2292Ile
NM_001375318.1:c.7034A>T	NP_001362247.1:p.Asn2345Ile
NM_003127.4:c.6920A>T	NP_003118.2:p.Asn2307Ile