Canonical Allele Identifier: CA353677910
Gene: ARL13B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.94035356G>C , CM000665.2:g.94035356G>C GRCh38
NC_000003.11:g.93754200G>C , CM000665.1:g.93754200G>C GRCh37
NC_000003.10:g.95236890G>C NCBI36
NG_017076.1:g.60218G>C

Transcript Alleles

HGVS Amino-acid Change
NM_001174150.2:c.406G>C MANE Select NP_001167621.1:p.Gly136Arg
ENST00000394222.8:c.406G>C MANE Select ENSP00000377769.3:p.Gly136Arg
NM_001174150.1:c.406G>C NP_001167621.1:p.Gly136Arg
NM_001174151.1:c.97G>C NP_001167622.1:p.Gly33Arg
NM_001174151.2:c.97G>C NP_001167622.1:p.Gly33Arg
NM_001321328.1:c.361G>C NP_001308257.1:p.Gly121Arg
NM_001321328.2:c.361G>C NP_001308257.1:p.Gly121Arg
NM_144996.3:c.85G>C NP_659433.2:p.Gly29Arg
NM_144996.4:c.85G>C NP_659433.2:p.Gly29Arg
NM_182896.2:c.406G>C NP_878899.1:p.Gly136Arg
NM_182896.3:c.406G>C NP_878899.1:p.Gly136Arg
NR_033427.1:n.441G>C
NR_033427.2:n.425G>C
NR_135621.1:n.437G>C
NR_135621.2:n.421G>C
ENST00000303097.11:c.85G>C ENSP00000306225.7:p.Gly29Arg
ENST00000335438.7:c.*258G>C ENSP00000335400.3:n.*258G>C
ENST00000394222.7:c.406G>C ENSP00000377769.3:p.Gly136Arg
ENST00000460371.5:c.131-1196G>C ENSP00000417263.1:n.131-1196G>C
ENST00000471138.5:c.406G>C ENSP00000420780.1:p.Gly136Arg
ENST00000486562.1:n.362G>C
ENST00000486562.2:c.85G>C ENSP00000505366.1:p.Gly29Arg
ENST00000535334.5:c.97G>C ENSP00000445145.1:p.Gly33Arg
ENST00000679404.1:c.331G>C ENSP00000505252.1:p.Gly111Arg
ENST00000679587.1:c.406G>C ENSP00000505396.1:p.Gly136Arg
ENST00000679601.1:c.*258G>C ENSP00000506200.1:n.*258G>C
ENST00000679607.1:c.-432G>C ENSP00000505148.1:n.-432G>C
ENST00000679654.1:c.*14G>C ENSP00000505178.1:n.*14G>C
ENST00000679657.1:c.-32-14050G>C ENSP00000505494.1:n.-32-14050G>C
ENST00000679666.1:c.34G>C ENSP00000506469.1:p.Gly12Arg
ENST00000679739.1:c.72-1196G>C ENSP00000506703.1:n.72-1196G>C
ENST00000679872.1:c.355G>C ENSP00000505607.1:p.Gly119Arg
ENST00000680414.1:c.*233-1196G>C ENSP00000506063.1:n.*233-1196G>C
ENST00000680430.1:c.655G>C ENSP00000504943.1:n.655G>C
ENST00000680994.1:n.436G>C
ENST00000681013.1:c.381-1196G>C ENSP00000506243.1:n.381-1196G>C
ENST00000681247.1:c.60-1196G>C ENSP00000505168.1:n.60-1196G>C
ENST00000681380.1:c.406G>C ENSP00000505402.1:p.Gly136Arg
ENST00000681655.1:c.331G>C ENSP00000505036.1:p.Gly111Arg
XM_006713531.2:c.361G>C XP_006713594.1:p.Gly121Arg
XM_006713532.2:c.361G>C XP_006713595.1:p.Gly121Arg
XM_006713532.3:c.361G>C XP_006713595.1:p.Gly121Arg
XM_011512532.1:c.370G>C XP_011510834.1:p.Gly124Arg
XM_011512532.2:c.370G>C XP_011510834.1:p.Gly124Arg
XM_011512533.1:c.370G>C XP_011510835.1:p.Gly124Arg
XM_011512533.2:c.370G>C XP_011510835.1:p.Gly124Arg
XM_011512534.1:c.361G>C XP_011510836.1:p.Gly121Arg
XM_011512534.2:c.361G>C XP_011510836.1:p.Gly121Arg
XM_011512535.1:c.331G>C XP_011510837.1:p.Gly111Arg
XM_011512535.2:c.331G>C XP_011510837.1:p.Gly111Arg
XM_011512536.1:c.97G>C XP_011510838.1:p.Gly33Arg
XM_017005853.1:c.97G>C XP_016861342.1:p.Gly33Arg