Canonical Allele Identifier: CA2504325
Community Standard Title: NM_001174150.2(ARL13B):c.1252C>T (p.Arg418Ter)
Gene: ARL13B HGNC NCBI
DHFR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.94053228C>T , CM000665.2:g.94053228C>T GRCh38
NC_000003.11:g.93772072C>T , CM000665.1:g.93772072C>T GRCh37
NC_000003.10:g.95254762C>T NCBI36
NG_017076.1:g.78090C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001174150.2:c.1252C>T (ARL13B) MANE Select NP_001167621.1:p.Arg418Ter
ENST00000394222.8:c.1252C>T (ARL13B) MANE Select ENSP00000377769.3:p.Arg418Ter
NM_001174150.1:c.1252C>T (ARL13B) NP_001167621.1:p.Arg418Ter
NM_001174151.1:c.943C>T (ARL13B) NP_001167622.1:p.Arg315Ter
NM_001174151.2:c.943C>T (ARL13B) NP_001167622.1:p.Arg315Ter
NM_001321328.1:c.1207C>T (ARL13B) NP_001308257.1:p.Arg403Ter
NM_001321328.2:c.1207C>T (ARL13B) NP_001308257.1:p.Arg403Ter
NM_144996.3:c.931C>T (ARL13B) NP_659433.2:p.Arg311Ter
NM_144996.4:c.931C>T (ARL13B) NP_659433.2:p.Arg311Ter
NM_182896.2:c.1252C>T (ARL13B) NP_878899.1:p.Arg418Ter
NM_182896.3:c.1252C>T (ARL13B) NP_878899.1:p.Arg418Ter
NR_033427.1:n.1292C>T (ARL13B)
NR_033427.2:n.1276C>T (ARL13B)
NR_135621.1:n.1283C>T (ARL13B)
NR_135621.2:n.1267C>T (ARL13B)
ENST00000303097.11:c.931C>T (ARL13B) ENSP00000306225.7:p.Arg311Ter
ENST00000335438.7:c.*1104C>T (ARL13B) ENSP00000335400.3:n.*1104C>T
ENST00000394222.7:c.1252C>T (ARL13B) ENSP00000377769.3:p.Arg418Ter
ENST00000460371.5:c.*725C>T (ARL13B) ENSP00000417263.1:n.*725C>T
ENST00000471138.5:c.1252C>T (ARL13B) ENSP00000420780.1:p.Arg418Ter
ENST00000481631.1:n.290-5050G>A (DHFR2)
ENST00000486562.2:c.862C>T (ARL13B) ENSP00000505366.1:p.Arg288Ter
ENST00000535334.5:c.943C>T (ARL13B) ENSP00000445145.1:p.Arg315Ter
ENST00000679404.1:c.1177C>T (ARL13B) ENSP00000505252.1:p.Arg393Ter
ENST00000679587.1:c.1183C>T (ARL13B) ENSP00000505396.1:p.Arg395Ter
ENST00000679601.1:c.*1104C>T (ARL13B) ENSP00000506200.1:n.*1104C>T
ENST00000679607.1:c.415C>T (ARL13B) ENSP00000505148.1:p.Arg139Ter
ENST00000679654.1:c.*860C>T (ARL13B) ENSP00000505178.1:n.*860C>T
ENST00000679657.1:c.196C>T (ARL13B) ENSP00000505494.1:p.Arg66Ter
ENST00000679666.1:c.880C>T (ARL13B) ENSP00000506469.1:p.Arg294Ter
ENST00000679739.1:c.*660C>T (ARL13B) ENSP00000506703.1:n.*660C>T
ENST00000679872.1:c.1201C>T (ARL13B) ENSP00000505607.1:p.Arg401Ter
ENST00000680414.1:c.*998C>T (ARL13B) ENSP00000506063.1:n.*998C>T
ENST00000680430.1:c.1501C>T (ARL13B) ENSP00000504943.1:n.1501C>T
ENST00000680994.1:n.1282C>T (ARL13B)
ENST00000681013.1:c.*660C>T (ARL13B) ENSP00000506243.1:n.*660C>T
ENST00000681247.1:c.*660C>T (ARL13B) ENSP00000505168.1:n.*660C>T
ENST00000681377.1:n.1584C>T (ARL13B)
ENST00000681380.1:c.1339C>T (ARL13B) ENSP00000505402.1:p.Arg447Ter
ENST00000681655.1:c.1177C>T (ARL13B) ENSP00000505036.1:p.Arg393Ter
XM_006713531.2:c.1207C>T (ARL13B) XP_006713594.1:p.Arg403Ter
XM_006713532.2:c.1207C>T (ARL13B) XP_006713595.1:p.Arg403Ter
XM_006713532.3:c.1207C>T (ARL13B) XP_006713595.1:p.Arg403Ter
XM_011512532.1:c.1216C>T (ARL13B) XP_011510834.1:p.Arg406Ter
XM_011512532.2:c.1216C>T (ARL13B) XP_011510834.1:p.Arg406Ter
XM_011512533.1:c.1216C>T (ARL13B) XP_011510835.1:p.Arg406Ter
XM_011512533.2:c.1216C>T (ARL13B) XP_011510835.1:p.Arg406Ter
XM_011512534.1:c.1207C>T (ARL13B) XP_011510836.1:p.Arg403Ter
XM_011512534.2:c.1207C>T (ARL13B) XP_011510836.1:p.Arg403Ter
XM_011512535.1:c.1177C>T (ARL13B) XP_011510837.1:p.Arg393Ter
XM_011512535.2:c.1177C>T (ARL13B) XP_011510837.1:p.Arg393Ter
XM_011512536.1:c.943C>T (ARL13B) XP_011510838.1:p.Arg315Ter
XM_017005853.1:c.943C>T (ARL13B) XP_016861342.1:p.Arg315Ter