Canonical Allele Identifier: CA353679432
Community Standard Title: NM_001174150.2(ARL13B):c.1067A>G (p.Asn356Ser)
Gene: ARL13B HGNC NCBI
DHFR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.94049448A>G , CM000665.2:g.94049448A>G GRCh38
NC_000003.11:g.93768292A>G , CM000665.1:g.93768292A>G GRCh37
NC_000003.10:g.95250982A>G NCBI36
NG_017076.1:g.74310A>G

Transcript Alleles

HGVS Amino-acid Change
NM_001174150.2:c.1067A>G (ARL13B) MANE Select NP_001167621.1:p.Asn356Ser
ENST00000394222.8:c.1067A>G (ARL13B) MANE Select ENSP00000377769.3:p.Asn356Ser
NM_001174150.1:c.1067A>G (ARL13B) NP_001167621.1:p.Asn356Ser
NM_001174151.1:c.758A>G (ARL13B) NP_001167622.1:p.Asn253Ser
NM_001174151.2:c.758A>G (ARL13B) NP_001167622.1:p.Asn253Ser
NM_001321328.1:c.1022A>G (ARL13B) NP_001308257.1:p.Asn341Ser
NM_001321328.2:c.1022A>G (ARL13B) NP_001308257.1:p.Asn341Ser
NM_144996.3:c.746A>G (ARL13B) NP_659433.2:p.Asn249Ser
NM_144996.4:c.746A>G (ARL13B) NP_659433.2:p.Asn249Ser
NM_182896.2:c.1067A>G (ARL13B) NP_878899.1:p.Asn356Ser
NM_182896.3:c.1067A>G (ARL13B) NP_878899.1:p.Asn356Ser
NR_033427.1:n.1107A>G (ARL13B)
NR_033427.2:n.1091A>G (ARL13B)
NR_135621.1:n.1098A>G (ARL13B)
NR_135621.2:n.1082A>G (ARL13B)
ENST00000303097.11:c.746A>G (ARL13B) ENSP00000306225.7:p.Asn249Ser
ENST00000335438.7:c.*919A>G (ARL13B) ENSP00000335400.3:n.*919A>G
ENST00000394222.7:c.1067A>G (ARL13B) ENSP00000377769.3:p.Asn356Ser
ENST00000460371.5:c.*540A>G (ARL13B) ENSP00000417263.1:n.*540A>G
ENST00000471138.5:c.1067A>G (ARL13B) ENSP00000420780.1:p.Asn356Ser
ENST00000481631.1:n.290-1270T>C (DHFR2)
ENST00000486562.2:c.746A>G (ARL13B) ENSP00000505366.1:p.Asn249Ser
ENST00000535334.5:c.758A>G (ARL13B) ENSP00000445145.1:p.Asn253Ser
ENST00000679404.1:c.992A>G (ARL13B) ENSP00000505252.1:p.Asn331Ser
ENST00000679587.1:c.1067A>G (ARL13B) ENSP00000505396.1:p.Asn356Ser
ENST00000679601.1:c.*919A>G (ARL13B) ENSP00000506200.1:n.*919A>G
ENST00000679607.1:c.230A>G (ARL13B) ENSP00000505148.1:p.Asn77Ser
ENST00000679654.1:c.*675A>G (ARL13B) ENSP00000505178.1:n.*675A>G
ENST00000679657.1:c.11A>G (ARL13B) ENSP00000505494.1:p.Asn4Ser
ENST00000679666.1:c.695A>G (ARL13B) ENSP00000506469.1:p.Asn232Ser
ENST00000679739.1:c.*475A>G (ARL13B) ENSP00000506703.1:n.*475A>G
ENST00000679872.1:c.1016A>G (ARL13B) ENSP00000505607.1:p.Asn339Ser
ENST00000680414.1:c.*813A>G (ARL13B) ENSP00000506063.1:n.*813A>G
ENST00000680430.1:c.1316A>G (ARL13B) ENSP00000504943.1:n.1316A>G
ENST00000680994.1:n.1097A>G (ARL13B)
ENST00000681013.1:c.*475A>G (ARL13B) ENSP00000506243.1:n.*475A>G
ENST00000681247.1:c.*475A>G (ARL13B) ENSP00000505168.1:n.*475A>G
ENST00000681377.1:n.1399A>G (ARL13B)
ENST00000681380.1:c.1154A>G (ARL13B) ENSP00000505402.1:p.Asn385Ser
ENST00000681655.1:c.992A>G (ARL13B) ENSP00000505036.1:p.Asn331Ser
XM_006713531.2:c.1022A>G (ARL13B) XP_006713594.1:p.Asn341Ser
XM_006713532.2:c.1022A>G (ARL13B) XP_006713595.1:p.Asn341Ser
XM_006713532.3:c.1022A>G (ARL13B) XP_006713595.1:p.Asn341Ser
XM_011512532.1:c.1031A>G (ARL13B) XP_011510834.1:p.Asn344Ser
XM_011512532.2:c.1031A>G (ARL13B) XP_011510834.1:p.Asn344Ser
XM_011512533.1:c.1031A>G (ARL13B) XP_011510835.1:p.Asn344Ser
XM_011512533.2:c.1031A>G (ARL13B) XP_011510835.1:p.Asn344Ser
XM_011512534.1:c.1022A>G (ARL13B) XP_011510836.1:p.Asn341Ser
XM_011512534.2:c.1022A>G (ARL13B) XP_011510836.1:p.Asn341Ser
XM_011512535.1:c.992A>G (ARL13B) XP_011510837.1:p.Asn331Ser
XM_011512535.2:c.992A>G (ARL13B) XP_011510837.1:p.Asn331Ser
XM_011512536.1:c.758A>G (ARL13B) XP_011510838.1:p.Asn253Ser
XM_017005853.1:c.758A>G (ARL13B) XP_016861342.1:p.Asn253Ser