Canonical Allele Identifier: CA2504301

Gene: ARL13B DHFR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.94050906A>G , CM000665.2:g.94050906A>G	GRCh38
NC_000003.11:g.93769750A>G , CM000665.1:g.93769750A>G	GRCh37
NC_000003.10:g.95252440A>G	NCBI36
NG_017076.1:g.75768A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001174150.2:c.1210+14A>G (ARL13B) MANE Select	NP_001167621.1:n.1210+14A>G
ENST00000394222.8:c.1210+14A>G (ARL13B) MANE Select	ENSP00000377769.3:n.1210+14A>G
NM_001174150.1:c.1210+14A>G (ARL13B)	NP_001167621.1:n.1210+14A>G
NM_001174151.1:c.901+14A>G (ARL13B)	NP_001167622.1:n.901+14A>G
NM_001174151.2:c.901+14A>G (ARL13B)	NP_001167622.1:n.901+14A>G
NM_001321328.1:c.1165+14A>G (ARL13B)	NP_001308257.1:n.1165+14A>G
NM_001321328.2:c.1165+14A>G (ARL13B)	NP_001308257.1:n.1165+14A>G
NM_144996.3:c.889+14A>G (ARL13B)	NP_659433.2:n.889+14A>G
NM_144996.4:c.889+14A>G (ARL13B)	NP_659433.2:n.889+14A>G
NM_182896.2:c.1210+14A>G (ARL13B)	NP_878899.1:n.1210+14A>G
NM_182896.3:c.1210+14A>G (ARL13B)	NP_878899.1:n.1210+14A>G
NR_033427.1:n.1250+14A>G (ARL13B)
NR_033427.2:n.1234+14A>G (ARL13B)
NR_135621.1:n.1241+14A>G (ARL13B)
NR_135621.2:n.1225+14A>G (ARL13B)
ENST00000303097.11:c.889+14A>G (ARL13B)	ENSP00000306225.7:n.889+14A>G
ENST00000335438.7:c.*1062+14A>G (ARL13B)	ENSP00000335400.3:n.*1062+14A>G
ENST00000394222.7:c.1210+14A>G (ARL13B)	ENSP00000377769.3:n.1210+14A>G
ENST00000460371.5:c.*683+14A>G (ARL13B)	ENSP00000417263.1:n.*683+14A>G
ENST00000471138.5:c.1210+14A>G (ARL13B)	ENSP00000420780.1:n.1210+14A>G
ENST00000481631.1:n.290-2728T>C (DHFR2)
ENST00000486562.2:c.820+1384A>G (ARL13B)	ENSP00000505366.1:n.820+1384A>G
ENST00000535334.5:c.901+14A>G (ARL13B)	ENSP00000445145.1:n.901+14A>G
ENST00000679404.1:c.1135+14A>G (ARL13B)	ENSP00000505252.1:n.1135+14A>G
ENST00000679587.1:c.1141+1384A>G (ARL13B)	ENSP00000505396.1:n.1141+1384A>G
ENST00000679601.1:c.*1062+14A>G (ARL13B)	ENSP00000506200.1:n.*1062+14A>G
ENST00000679607.1:c.373+14A>G (ARL13B)	ENSP00000505148.1:n.373+14A>G
ENST00000679654.1:c.*818+14A>G (ARL13B)	ENSP00000505178.1:n.*818+14A>G
ENST00000679657.1:c.154+14A>G (ARL13B)	ENSP00000505494.1:n.154+14A>G
ENST00000679666.1:c.838+14A>G (ARL13B)	ENSP00000506469.1:n.838+14A>G
ENST00000679739.1:c.*618+14A>G (ARL13B)	ENSP00000506703.1:n.*618+14A>G
ENST00000679872.1:c.1159+14A>G (ARL13B)	ENSP00000505607.1:n.1159+14A>G
ENST00000680414.1:c.*956+14A>G (ARL13B)	ENSP00000506063.1:n.*956+14A>G
ENST00000680430.1:c.1459+14A>G (ARL13B)	ENSP00000504943.1:n.1459+14A>G
ENST00000680994.1:n.1240+14A>G (ARL13B)
ENST00000681013.1:c.*618+14A>G (ARL13B)	ENSP00000506243.1:n.*618+14A>G
ENST00000681247.1:c.*618+14A>G (ARL13B)	ENSP00000505168.1:n.*618+14A>G
ENST00000681377.1:n.1542+14A>G (ARL13B)
ENST00000681380.1:c.1297+14A>G (ARL13B)	ENSP00000505402.1:n.1297+14A>G
ENST00000681655.1:c.1135+14A>G (ARL13B)	ENSP00000505036.1:n.1135+14A>G
XM_006713531.2:c.1165+14A>G (ARL13B)	XP_006713594.1:n.1165+14A>G
XM_006713532.2:c.1165+14A>G (ARL13B)	XP_006713595.1:n.1165+14A>G
XM_006713532.3:c.1165+14A>G (ARL13B)	XP_006713595.1:n.1165+14A>G
XM_011512532.1:c.1174+14A>G (ARL13B)	XP_011510834.1:n.1174+14A>G
XM_011512532.2:c.1174+14A>G (ARL13B)	XP_011510834.1:n.1174+14A>G
XM_011512533.1:c.1174+14A>G (ARL13B)	XP_011510835.1:n.1174+14A>G
XM_011512533.2:c.1174+14A>G (ARL13B)	XP_011510835.1:n.1174+14A>G
XM_011512534.1:c.1165+14A>G (ARL13B)	XP_011510836.1:n.1165+14A>G
XM_011512534.2:c.1165+14A>G (ARL13B)	XP_011510836.1:n.1165+14A>G
XM_011512535.1:c.1135+14A>G (ARL13B)	XP_011510837.1:n.1135+14A>G
XM_011512535.2:c.1135+14A>G (ARL13B)	XP_011510837.1:n.1135+14A>G
XM_011512536.1:c.901+14A>G (ARL13B)	XP_011510838.1:n.901+14A>G
XM_017005853.1:c.901+14A>G (ARL13B)	XP_016861342.1:n.901+14A>G