Canonical Allele Identifier: CA1880371251
Gene: SPTAN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.128632222G= , CM000671.2:g.128632222G= GRCh38
NC_000009.11:g.131394501G= , CM000671.1:g.131394501G= GRCh37
NC_000009.10:g.130434322G= NCBI36
NG_027748.1:g.84665G=
NG_034056.1:g.29629C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000627441.3:c.6894G= ENSP00000486547.2:p.Lys2298=
ENST00000630866.2:c.6921G= ENSP00000487444.1:p.Lys2307=
ENST00000704202.1:c.6945G= ENSP00000515764.1:p.Lys2315=
ENST00000704203.1:c.6894G= ENSP00000515765.1:p.Lys2298=
ENST00000704204.1:c.6384G= ENSP00000515766.1:p.Lys2128=
ENST00000704206.1:c.4463G=
ENST00000704207.1:c.2800G=
ENST00000706487.1:c.6858G= ENSP00000516412.1:p.Lys2286=
ENST00000372739.7:c.6858G= MANE Select ENSP00000361824.4:p.Lys2286=
ENST00000636010.1:n.582G=
ENST00000358161.9:c.6783G= ENSP00000350882.6:p.Lys2261=
ENST00000372731.8:c.6843G= ENSP00000361816.4:p.Lys2281=
ENST00000372739.5:c.6858G= ENSP00000361824.3:p.Lys2286=
ENST00000625980.2:n.812G=
ENST00000630763.1:n.615G=
ENST00000630804.2:c.6798G= ENSP00000486308.1:p.Lys2266=
ENST00000630866.1:c.6921G= ENSP00000487444.1:p.Lys2307=
NM_001130438.2:c.6858G= NP_001123910.1:p.Lys2286=
NM_001195532.1:c.6783G= NP_001182461.1:p.Lys2261=
NM_003127.3:c.6843G= NP_003118.2:p.Lys2281=
XM_006717245.1:c.6957G= XP_006717308.1:p.Lys2319=
XM_006717246.1:c.6942G= XP_006717309.1:p.Lys2314=
XM_006717247.1:c.6897G= XP_006717310.1:p.Lys2299=
XM_006717248.1:c.6894G= XP_006717311.1:p.Lys2298=
XM_006717249.1:c.6879G= XP_006717312.1:p.Lys2293=
XM_006717250.1:c.6876G= XP_006717313.1:p.Lys2292=
XM_006717251.1:c.6861G= XP_006717314.1:p.Lys2287=
XM_006717252.1:c.6834G= XP_006717315.1:p.Lys2278=
XM_006717253.1:c.6819G= XP_006717316.1:p.Lys2273=
XM_006717254.1:c.6921G= XP_006717317.1:p.Lys2307=
NM_001363759.1:c.6921G= NP_001350688.1:p.Lys2307=
NM_001363765.1:c.6798G= NP_001350694.1:p.Lys2266=
XM_006717247.2:c.6897G= XP_006717310.1:p.Lys2299=
XM_006717248.2:c.6894G= XP_006717311.1:p.Lys2298=
XM_006717251.2:c.6861G= XP_006717314.1:p.Lys2287=
XM_006717252.3:c.6834G= XP_006717315.1:p.Lys2278=
XM_017015059.1:c.6840G= XP_016870548.1:p.Lys2280=
XM_017015060.1:c.6816G= XP_016870549.1:p.Lys2272=
NM_001130438.3:c.6858G= MANE Select NP_001123910.1:p.Lys2286=
NM_001195532.2:c.6783G= NP_001182461.1:p.Lys2261=
NM_001363759.2:c.6921G= NP_001350688.1:p.Lys2307=
NM_001363765.2:c.6798G= NP_001350694.1:p.Lys2266=
NM_001375310.1:c.6945G= NP_001362239.1:p.Lys2315=
NM_001375311.2:c.6858G= NP_001362240.1:p.Lys2286=
NM_001375312.2:c.6894G= NP_001362241.2:p.Lys2298=
NM_001375313.1:c.6840G= NP_001362242.1:p.Lys2280=
NM_001375314.2:c.6798G= NP_001362243.1:p.Lys2266=
NM_001375318.1:c.6957G= NP_001362247.1:p.Lys2319=
NM_003127.4:c.6843G= NP_003118.2:p.Lys2281=