Canonical Allele Identifier: CA2580070629

Gene: ARL13B

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93995856A>G , CM000665.2:g.93995856A>G	GRCh38
NC_000003.11:g.93714700A>G , CM000665.1:g.93714700A>G	GRCh37
NC_000003.10:g.95197390A>G	NCBI36
NG_017076.1:g.20718A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394222.8:c.60-18A>G MANE Select	ENSP00000377769.3:n.60-18A>G
ENST00000475206.3:n.155-18A>G
ENST00000486562.2:c.59+15374A>G	ENSP00000505366.1:n.59+15374A>G
ENST00000492165.3:n.342-18A>G
ENST00000679404.1:c.-16-18A>G	ENSP00000505252.1:n.-16-18A>G
ENST00000679587.1:c.60-18A>G	ENSP00000505396.1:n.60-18A>G
ENST00000679601.1:c.60-18A>G	ENSP00000506200.1:n.60-18A>G
ENST00000679607.1:c.-458+7145A>G	ENSP00000505148.1:n.-458+7145A>G
ENST00000679654.1:c.60-18A>G	ENSP00000505178.1:n.60-18A>G
ENST00000679657.1:c.-33+15374A>G	ENSP00000505494.1:n.-33+15374A>G
ENST00000679666.1:c.8+6740A>G	ENSP00000506469.1:n.8+6740A>G
ENST00000679739.1:c.-179-7803A>G	ENSP00000506703.1:n.-179-7803A>G
ENST00000679872.1:c.9-18A>G	ENSP00000505607.1:n.9-18A>G
ENST00000680414.1:c.60-18A>G	ENSP00000506063.1:n.60-18A>G
ENST00000680430.1:c.60-18A>G	ENSP00000504943.1:n.60-18A>G
ENST00000680994.1:n.340-18A>G
ENST00000681013.1:c.60-18A>G	ENSP00000506243.1:n.60-18A>G
ENST00000681247.1:c.59+15374A>G	ENSP00000505168.1:n.59+15374A>G
ENST00000681380.1:c.60-18A>G	ENSP00000505402.1:n.60-18A>G
ENST00000681655.1:c.-16-18A>G	ENSP00000505036.1:n.-16-18A>G
ENST00000303097.11:c.59+15374A>G	ENSP00000306225.7:n.59+15374A>G
ENST00000335438.7:c.60-18A>G	ENSP00000335400.3:n.60-18A>G
ENST00000394222.7:c.60-18A>G	ENSP00000377769.3:n.60-18A>G
ENST00000460371.5:c.60-18A>G	ENSP00000417263.1:n.60-18A>G
ENST00000471138.5:c.60-18A>G	ENSP00000420780.1:n.60-18A>G
ENST00000475206.2:n.214-18A>G
ENST00000478400.3:n.382-18A>G
ENST00000486562.1:n.270-22A>G
ENST00000492165.2:n.196-7803A>G
ENST00000535334.5:c.-179-7803A>G	ENSP00000445145.1:n.-179-7803A>G
NM_001174150.1:c.60-18A>G	NP_001167621.1:n.60-18A>G
NM_001174151.1:c.-179-7803A>G	NP_001167622.1:n.-179-7803A>G
NM_144996.3:c.59+15374A>G	NP_659433.2:n.59+15374A>G
NM_182896.2:c.60-18A>G	NP_878899.1:n.60-18A>G
NR_033427.1:n.345-18A>G
XM_006713531.2:c.-108-18A>G	XP_006713594.1:n.-108-18A>G
XM_006713532.2:c.-123-18A>G	XP_006713595.1:n.-123-18A>G
XM_011512532.1:c.-32-18A>G	XP_011510834.1:n.-32-18A>G
XM_011512533.1:c.-32-18A>G	XP_011510835.1:n.-32-18A>G
XM_011512534.1:c.-108-18A>G	XP_011510836.1:n.-108-18A>G
XM_011512535.1:c.-16-18A>G	XP_011510837.1:n.-16-18A>G
NM_001321328.1:c.-108-18A>G	NP_001308257.1:n.-108-18A>G
NR_135621.1:n.345-22A>G
XM_006713532.3:c.-123-18A>G	XP_006713595.1:n.-123-18A>G
XM_011512532.2:c.-32-18A>G	XP_011510834.1:n.-32-18A>G
XM_011512533.2:c.-32-18A>G	XP_011510835.1:n.-32-18A>G
XM_011512534.2:c.-108-18A>G	XP_011510836.1:n.-108-18A>G
XM_011512535.2:c.-16-18A>G	XP_011510837.1:n.-16-18A>G
XM_017005853.1:c.-307-18A>G	XP_016861342.1:n.-307-18A>G
NM_001174150.2:c.60-18A>G MANE Select	NP_001167621.1:n.60-18A>G
NM_001321328.2:c.-108-18A>G	NP_001308257.1:n.-108-18A>G
NM_144996.4:c.59+15374A>G	NP_659433.2:n.59+15374A>G
NM_182896.3:c.60-18A>G	NP_878899.1:n.60-18A>G
NR_033427.2:n.329-18A>G
NR_135621.2:n.329-22A>G
NM_001174151.2:c.-179-7803A>G	NP_001167622.1:n.-179-7803A>G