Canonical Allele Identifier: CA1880371313
Gene: SPTAN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.128632380A= , CM000671.2:g.128632380A= GRCh38
NC_000009.11:g.131394659A= , CM000671.1:g.131394659A= GRCh37
NC_000009.10:g.130434480A= NCBI36
NG_027748.1:g.84823A=
NG_034056.1:g.29471T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000627441.3:c.6996-51A= ENSP00000486547.2:n.6996-51A=
ENST00000630866.2:c.7023-51A= ENSP00000487444.1:n.7023-51A=
ENST00000704202.1:c.7047-51A= ENSP00000515764.1:n.7047-51A=
ENST00000704203.1:c.6996-51A= ENSP00000515765.1:n.6996-51A=
ENST00000704204.1:c.6486-51A= ENSP00000515766.1:n.6486-51A=
ENST00000704206.1:c.4565-51A=
ENST00000704207.1:c.2902-51A=
ENST00000706487.1:c.6960-51A= ENSP00000516412.1:n.6960-51A=
ENST00000372739.7:c.6960-51A= MANE Select ENSP00000361824.4:n.6960-51A=
ENST00000636010.1:n.684-51A=
ENST00000358161.9:c.6885-51A= ENSP00000350882.6:n.6885-51A=
ENST00000372731.8:c.6945-51A= ENSP00000361816.4:n.6945-51A=
ENST00000372739.5:c.6960-51A= ENSP00000361824.3:n.6960-51A=
ENST00000625980.2:n.914-51A=
ENST00000630763.1:n.717-51A=
ENST00000630804.2:c.6900-51A= ENSP00000486308.1:n.6900-51A=
ENST00000630866.1:c.7023-51A= ENSP00000487444.1:n.7023-51A=
NM_001130438.2:c.6960-51A= NP_001123910.1:n.6960-51A=
NM_001195532.1:c.6885-51A= NP_001182461.1:n.6885-51A=
NM_003127.3:c.6945-51A= NP_003118.2:n.6945-51A=
XM_006717245.1:c.7059-51A= XP_006717308.1:n.7059-51A=
XM_006717246.1:c.7044-51A= XP_006717309.1:n.7044-51A=
XM_006717247.1:c.6999-51A= XP_006717310.1:n.6999-51A=
XM_006717248.1:c.6996-51A= XP_006717311.1:n.6996-51A=
XM_006717249.1:c.6981-51A= XP_006717312.1:n.6981-51A=
XM_006717250.1:c.6978-51A= XP_006717313.1:n.6978-51A=
XM_006717251.1:c.6963-51A= XP_006717314.1:n.6963-51A=
XM_006717252.1:c.6936-51A= XP_006717315.1:n.6936-51A=
XM_006717253.1:c.6921-51A= XP_006717316.1:n.6921-51A=
XM_006717254.1:c.7023-51A= XP_006717317.1:n.7023-51A=
NM_001363759.1:c.7023-51A= NP_001350688.1:n.7023-51A=
NM_001363765.1:c.6900-51A= NP_001350694.1:n.6900-51A=
XM_006717247.2:c.6999-51A= XP_006717310.1:n.6999-51A=
XM_006717248.2:c.6996-51A= XP_006717311.1:n.6996-51A=
XM_006717251.2:c.6963-51A= XP_006717314.1:n.6963-51A=
XM_006717252.3:c.6936-51A= XP_006717315.1:n.6936-51A=
XM_017015059.1:c.6942-51A= XP_016870548.1:n.6942-51A=
XM_017015060.1:c.6918-51A= XP_016870549.1:n.6918-51A=
NM_001130438.3:c.6960-51A= MANE Select NP_001123910.1:n.6960-51A=
NM_001195532.2:c.6885-51A= NP_001182461.1:n.6885-51A=
NM_001363759.2:c.7023-51A= NP_001350688.1:n.7023-51A=
NM_001363765.2:c.6900-51A= NP_001350694.1:n.6900-51A=
NM_001375310.1:c.7047-51A= NP_001362239.1:n.7047-51A=
NM_001375311.2:c.6960-51A= NP_001362240.1:n.6960-51A=
NM_001375312.2:c.6996-51A= NP_001362241.2:n.6996-51A=
NM_001375313.1:c.6942-51A= NP_001362242.1:n.6942-51A=
NM_001375314.2:c.6900-51A= NP_001362243.1:n.6900-51A=
NM_001375318.1:c.7059-51A= NP_001362247.1:n.7059-51A=
NM_003127.4:c.6945-51A= NP_003118.2:n.6945-51A=