Canonical Allele Identifier: CA353675123

Gene: ARL13B

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93980483G>A , CM000665.2:g.93980483G>A	GRCh38
NC_000003.11:g.93699327G>A , CM000665.1:g.93699327G>A	GRCh37
NC_000003.10:g.95182017G>A	NCBI36
NG_017076.1:g.5345G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001174150.2:c.59+1G>A MANE Select	NP_001167621.1:n.59+1G>A
ENST00000394222.8:c.59+1G>A MANE Select	ENSP00000377769.3:n.59+1G>A
NM_001174150.1:c.59+1G>A	NP_001167621.1:n.59+1G>A
NM_001174151.1:c.-180+1G>A	NP_001167622.1:n.-180+1G>A
NM_001174151.2:c.-180+1G>A	NP_001167622.1:n.-180+1G>A
NM_001321328.1:c.-109+1G>A	NP_001308257.1:n.-109+1G>A
NM_001321328.2:c.-109+1G>A	NP_001308257.1:n.-109+1G>A
NM_144996.3:c.59+1G>A	NP_659433.2:n.59+1G>A
NM_144996.4:c.59+1G>A	NP_659433.2:n.59+1G>A
NM_182896.2:c.59+1G>A	NP_878899.1:n.59+1G>A
NM_182896.3:c.59+1G>A	NP_878899.1:n.59+1G>A
NR_033427.1:n.344+1G>A
NR_033427.2:n.328+1G>A
NR_135621.1:n.344+1G>A
NR_135621.2:n.328+1G>A
ENST00000303097.11:c.59+1G>A	ENSP00000306225.7:n.59+1G>A
ENST00000335438.7:c.59+1G>A	ENSP00000335400.3:n.59+1G>A
ENST00000394222.7:c.59+1G>A	ENSP00000377769.3:n.59+1G>A
ENST00000460371.5:c.59+1G>A	ENSP00000417263.1:n.59+1G>A
ENST00000471138.5:c.59+1G>A	ENSP00000420780.1:n.59+1G>A
ENST00000475206.2:n.213+1G>A
ENST00000475206.3:n.154+1G>A
ENST00000478400.3:n.341+1G>A
ENST00000486562.1:n.269+1G>A
ENST00000486562.2:c.59+1G>A	ENSP00000505366.1:n.59+1G>A
ENST00000492165.2:n.195+1G>A
ENST00000492165.3:n.341+1G>A
ENST00000535334.5:c.-180+1G>A	ENSP00000445145.1:n.-180+1G>A
ENST00000679404.1:c.-296+1G>A	ENSP00000505252.1:n.-296+1G>A
ENST00000679587.1:c.59+1G>A	ENSP00000505396.1:n.59+1G>A
ENST00000679601.1:c.59+1G>A	ENSP00000506200.1:n.59+1G>A
ENST00000679607.1:c.-498+1G>A	ENSP00000505148.1:n.-498+1G>A
ENST00000679654.1:c.59+1G>A	ENSP00000505178.1:n.59+1G>A
ENST00000679657.1:c.-33+1G>A	ENSP00000505494.1:n.-33+1G>A
ENST00000679666.1:c.-291+1G>A	ENSP00000506469.1:n.-291+1G>A
ENST00000679739.1:c.-180+1G>A	ENSP00000506703.1:n.-180+1G>A
ENST00000679872.1:c.-291+1G>A	ENSP00000505607.1:n.-291+1G>A
ENST00000680414.1:c.59+1G>A	ENSP00000506063.1:n.59+1G>A
ENST00000680430.1:c.59+1G>A	ENSP00000504943.1:n.59+1G>A
ENST00000680994.1:n.339+1G>A
ENST00000681013.1:c.59+1G>A	ENSP00000506243.1:n.59+1G>A
ENST00000681247.1:c.59+1G>A	ENSP00000505168.1:n.59+1G>A
ENST00000681380.1:c.59+1G>A	ENSP00000505402.1:n.59+1G>A
ENST00000681655.1:c.-57+1G>A	ENSP00000505036.1:n.-57+1G>A
XM_006713531.2:c.-109+1G>A	XP_006713594.1:n.-109+1G>A
XM_006713532.2:c.-124+1G>A	XP_006713595.1:n.-124+1G>A
XM_006713532.3:c.-124+1G>A	XP_006713595.1:n.-124+1G>A
XM_011512532.1:c.-33+1G>A	XP_011510834.1:n.-33+1G>A
XM_011512532.2:c.-33+1G>A	XP_011510834.1:n.-33+1G>A
XM_011512533.1:c.-73+1G>A	XP_011510835.1:n.-73+1G>A
XM_011512533.2:c.-73+1G>A	XP_011510835.1:n.-73+1G>A
XM_011512534.1:c.-149+1G>A	XP_011510836.1:n.-149+1G>A
XM_011512534.2:c.-149+1G>A	XP_011510836.1:n.-149+1G>A
XM_011512535.1:c.-57+1G>A	XP_011510837.1:n.-57+1G>A
XM_011512535.2:c.-57+1G>A	XP_011510837.1:n.-57+1G>A
XM_017005853.1:c.-308+1G>A	XP_016861342.1:n.-308+1G>A