Canonical Allele Identifier: CA1880371240
Gene: SPTAN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.128632192C= , CM000671.2:g.128632192C= GRCh38
NC_000009.11:g.131394471C= , CM000671.1:g.131394471C= GRCh37
NC_000009.10:g.130434292C= NCBI36
NG_027748.1:g.84635C=
NG_034056.1:g.29659G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000627441.3:c.6864C= ENSP00000486547.2:p.Ala2288=
ENST00000630866.2:c.6891C= ENSP00000487444.1:p.Ala2297=
ENST00000704202.1:c.6915C= ENSP00000515764.1:p.Ala2305=
ENST00000704203.1:c.6864C= ENSP00000515765.1:p.Ala2288=
ENST00000704204.1:c.6354C= ENSP00000515766.1:p.Ala2118=
ENST00000704206.1:c.4433C=
ENST00000704207.1:c.2770C=
ENST00000706487.1:c.6828C= ENSP00000516412.1:p.Ala2276=
ENST00000372739.7:c.6828C= MANE Select ENSP00000361824.4:p.Ala2276=
ENST00000636010.1:n.552C=
ENST00000358161.9:c.6753C= ENSP00000350882.6:p.Ala2251=
ENST00000372731.8:c.6813C= ENSP00000361816.4:p.Ala2271=
ENST00000372739.5:c.6828C= ENSP00000361824.3:p.Ala2276=
ENST00000625980.2:n.782C=
ENST00000630763.1:n.585C=
ENST00000630804.2:c.6768C= ENSP00000486308.1:p.Ala2256=
ENST00000630866.1:c.6891C= ENSP00000487444.1:p.Ala2297=
NM_001130438.2:c.6828C= NP_001123910.1:p.Ala2276=
NM_001195532.1:c.6753C= NP_001182461.1:p.Ala2251=
NM_003127.3:c.6813C= NP_003118.2:p.Ala2271=
XM_006717245.1:c.6927C= XP_006717308.1:p.Ala2309=
XM_006717246.1:c.6912C= XP_006717309.1:p.Ala2304=
XM_006717247.1:c.6867C= XP_006717310.1:p.Ala2289=
XM_006717248.1:c.6864C= XP_006717311.1:p.Ala2288=
XM_006717249.1:c.6849C= XP_006717312.1:p.Ala2283=
XM_006717250.1:c.6846C= XP_006717313.1:p.Ala2282=
XM_006717251.1:c.6831C= XP_006717314.1:p.Ala2277=
XM_006717252.1:c.6804C= XP_006717315.1:p.Ala2268=
XM_006717253.1:c.6789C= XP_006717316.1:p.Ala2263=
XM_006717254.1:c.6891C= XP_006717317.1:p.Ala2297=
NM_001363759.1:c.6891C= NP_001350688.1:p.Ala2297=
NM_001363765.1:c.6768C= NP_001350694.1:p.Ala2256=
XM_006717247.2:c.6867C= XP_006717310.1:p.Ala2289=
XM_006717248.2:c.6864C= XP_006717311.1:p.Ala2288=
XM_006717251.2:c.6831C= XP_006717314.1:p.Ala2277=
XM_006717252.3:c.6804C= XP_006717315.1:p.Ala2268=
XM_017015059.1:c.6810C= XP_016870548.1:p.Ala2270=
XM_017015060.1:c.6786C= XP_016870549.1:p.Ala2262=
NM_001130438.3:c.6828C= MANE Select NP_001123910.1:p.Ala2276=
NM_001195532.2:c.6753C= NP_001182461.1:p.Ala2251=
NM_001363759.2:c.6891C= NP_001350688.1:p.Ala2297=
NM_001363765.2:c.6768C= NP_001350694.1:p.Ala2256=
NM_001375310.1:c.6915C= NP_001362239.1:p.Ala2305=
NM_001375311.2:c.6828C= NP_001362240.1:p.Ala2276=
NM_001375312.2:c.6864C= NP_001362241.2:p.Ala2288=
NM_001375313.1:c.6810C= NP_001362242.1:p.Ala2270=
NM_001375314.2:c.6768C= NP_001362243.1:p.Ala2256=
NM_001375318.1:c.6927C= NP_001362247.1:p.Ala2309=
NM_003127.4:c.6813C= NP_003118.2:p.Ala2271=