Canonical Allele Identifier: CA2505987
Community Standard Title: NM_001278293.3(ARL6):c.499G>A (p.Gly167Arg)
Gene: ARL6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.97791790G>A , CM000665.2:g.97791790G>A GRCh38
NC_000003.11:g.97510634G>A , CM000665.1:g.97510634G>A GRCh37
NC_000003.10:g.98993324G>A NCBI36
NG_008119.1:g.32040G>A
NG_008119.2:g.32040G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001278293.3:c.499G>A MANE Select NP_001265222.1:p.Gly167Arg
ENST00000463745.6:c.499G>A MANE Select ENSP00000419619.1:p.Gly167Arg
NM_001278293.1:c.499G>A NP_001265222.1:p.Gly167Arg
NM_001278293.2:c.499G>A NP_001265222.1:p.Gly167Arg
NM_001323513.1:c.499G>A NP_001310442.1:p.Gly167Arg
NM_001323513.2:c.499G>A NP_001310442.1:p.Gly167Arg
NM_001323514.1:c.479+3671G>A NP_001310443.1:n.479+3671G>A
NM_001323514.2:c.479+3671G>A NP_001310443.1:n.479+3671G>A
NM_032146.4:c.499G>A NP_115522.1:p.Gly167Arg
NM_032146.5:c.499G>A NP_115522.1:p.Gly167Arg
NM_177976.2:c.499G>A NP_816931.1:p.Gly167Arg
NM_177976.3:c.499G>A NP_816931.1:p.Gly167Arg
NR_103511.1:n.1082G>A
NR_103511.2:n.845G>A
NR_103511.3:n.845G>A
NR_136595.1:n.1639G>A
NR_136595.2:n.1402G>A
NR_136597.1:n.1540G>A
NR_136597.2:n.1303G>A
NR_136598.1:n.987G>A
NR_136598.2:n.750G>A
NR_136600.1:n.983G>A
NR_136600.2:n.746G>A
NR_136600.3:n.746G>A
NR_136601.1:n.983G>A
NR_136601.2:n.746G>A
NR_136601.3:n.746G>A
NR_136602.1:n.963+3671G>A
NR_136602.2:n.726+3671G>A
NR_136602.3:n.726+3671G>A
ENST00000335979.6:c.499G>A ENSP00000337722.2:p.Gly167Arg
ENST00000394206.5:c.499G>A ENSP00000377756.1:p.Gly167Arg
ENST00000462412.3:c.499G>A ENSP00000418740.2:p.Gly167Arg
ENST00000463745.5:c.499G>A ENSP00000419619.1:p.Gly167Arg
ENST00000476753.1:c.163+3671G>A
ENST00000493990.5:c.499G>A ENSP00000418057.1:p.Gly167Arg
ENST00000631834.1:c.361G>A ENSP00000488530.1:p.Gly121Arg
ENST00000631834.2:c.499G>A ENSP00000488530.2:p.Gly167Arg
XM_006713779.2:c.499G>A XP_006713842.1:p.Gly167Arg
XM_006713783.2:c.479+3671G>A XP_006713846.1:n.479+3671G>A
XM_017007311.2:c.499G>A XP_016862800.1:p.Gly167Arg
XM_017007312.2:c.479+3671G>A XP_016862801.1:n.479+3671G>A
XR_001740319.2:n.2923G>A
XR_001740321.2:n.2923G>A
XR_002959599.1:n.3539G>A
XR_924184.1:n.971G>A
XR_924184.3:n.2923G>A
XR_924185.1:n.1077G>A
XR_924185.3:n.3022G>A
XR_924186.1:n.1124G>A
XR_924186.3:n.3081G>A
XR_924187.1:n.971G>A
XR_924187.3:n.2923G>A
XR_924188.1:n.1025G>A
XR_924188.3:n.2982G>A
XR_924189.1:n.971G>A
XR_924189.3:n.2923G>A