Canonical Allele Identifier: CA1880364351
Gene: SPTAN1 HGNC NCBI

Linked Data

dbSNP Id: rs1857393833

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.128618060_128618069dup , CM000671.2:g.128618060_128618069dup GRCh38
NC_000009.11:g.131380339_131380348dup , CM000671.1:g.131380339_131380348dup GRCh37
NC_000009.10:g.130420160_130420169dup NCBI36
NG_027748.1:g.70503_70512dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000627441.3:c.5588_5597dup ENSP00000486547.2:p.Glu1867AlafsTer?
ENST00000630866.2:c.5552_5561dup ENSP00000487444.1:p.Glu1855AlafsTer?
ENST00000704202.1:c.5552_5561dup ENSP00000515764.1:p.Glu1855AlafsTer?
ENST00000704203.1:c.5588_5597dup ENSP00000515765.1:p.Glu1867AlafsTer?
ENST00000704204.1:c.5015_5024dup ENSP00000515766.1:p.Glu1676AlafsTer?
ENST00000704206.1:c.3175_3184dup
ENST00000704207.1:c.1162_1171dup
ENST00000706487.1:c.5552_5561dup ENSP00000516412.1:p.Glu1855AlafsTer?
ENST00000372739.7:c.5552_5561dup MANE Select ENSP00000361824.4:p.Glu1855AlafsTer?
ENST00000637434.1:n.780_789dup
ENST00000358161.9:c.5477_5486dup ENSP00000350882.6:p.Glu1830AlafsTer?
ENST00000372731.8:c.5537_5546dup ENSP00000361816.4:p.Glu1850AlafsTer?
ENST00000372739.5:c.5552_5561dup ENSP00000361824.3:p.Glu1855AlafsTer?
ENST00000630804.2:c.5492_5501dup ENSP00000486308.1:p.Glu1835AlafsTer?
ENST00000630866.1:c.5552_5561dup ENSP00000487444.1:p.Glu1855AlafsTer?
NM_001130438.2:c.5552_5561dup NP_001123910.1:p.Glu1855AlafsTer?
NM_001195532.1:c.5477_5486dup NP_001182461.1:p.Glu1830AlafsTer?
NM_003127.3:c.5537_5546dup NP_003118.2:p.Glu1850AlafsTer?
XM_006717245.1:c.5588_5597dup XP_006717308.1:p.Glu1867AlafsTer?
XM_006717246.1:c.5573_5582dup XP_006717309.1:p.Glu1862AlafsTer?
XM_006717247.1:c.5528_5537dup XP_006717310.1:p.Glu1847AlafsTer?
XM_006717248.1:c.5588_5597dup XP_006717311.1:p.Glu1867AlafsTer?
XM_006717249.1:c.5573_5582dup XP_006717312.1:p.Glu1862AlafsTer?
XM_006717250.1:c.5588_5597dup XP_006717313.1:p.Glu1867AlafsTer?
XM_006717251.1:c.5492_5501dup XP_006717314.1:p.Glu1835AlafsTer?
XM_006717252.1:c.5528_5537dup XP_006717315.1:p.Glu1847AlafsTer?
XM_006717253.1:c.5513_5522dup XP_006717316.1:p.Glu1842AlafsTer?
XM_006717254.1:c.5552_5561dup XP_006717317.1:p.Glu1855AlafsTer?
NM_001363759.1:c.5552_5561dup NP_001350688.1:p.Glu1855AlafsTer?
NM_001363765.1:c.5492_5501dup NP_001350694.1:p.Glu1835AlafsTer?
XM_006717247.2:c.5528_5537dup XP_006717310.1:p.Glu1847AlafsTer?
XM_006717248.2:c.5588_5597dup XP_006717311.1:p.Glu1867AlafsTer?
XM_006717251.2:c.5492_5501dup XP_006717314.1:p.Glu1835AlafsTer?
XM_006717252.3:c.5528_5537dup XP_006717315.1:p.Glu1847AlafsTer?
XM_017015059.1:c.5552_5561dup XP_016870548.1:p.Glu1855AlafsTer?
XM_017015060.1:c.5528_5537dup XP_016870549.1:p.Glu1847AlafsTer?
NM_001130438.3:c.5552_5561dup MANE Select NP_001123910.1:p.Glu1855AlafsTer?
NM_001195532.2:c.5477_5486dup NP_001182461.1:p.Glu1830AlafsTer?
NM_001363759.2:c.5552_5561dup NP_001350688.1:p.Glu1855AlafsTer?
NM_001363765.2:c.5492_5501dup NP_001350694.1:p.Glu1835AlafsTer?
NM_001375310.1:c.5552_5561dup NP_001362239.1:p.Glu1855AlafsTer?
NM_001375311.2:c.5552_5561dup NP_001362240.1:p.Glu1855AlafsTer?
NM_001375312.2:c.5588_5597dup NP_001362241.2:p.Glu1867AlafsTer?
NM_001375313.1:c.5552_5561dup NP_001362242.1:p.Glu1855AlafsTer?
NM_001375314.2:c.5492_5501dup NP_001362243.1:p.Glu1835AlafsTer?
NM_001375318.1:c.5588_5597dup NP_001362247.1:p.Glu1867AlafsTer?
NM_003127.4:c.5537_5546dup NP_003118.2:p.Glu1850AlafsTer?