Canonical Allele Identifier: CA2505958
Community Standard Title: NM_001278293.3(ARL6):c.442T>G (p.Cys148Gly)
Gene: ARL6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.97788082T>G , CM000665.2:g.97788082T>G GRCh38
NC_000003.11:g.97506926T>G , CM000665.1:g.97506926T>G GRCh37
NC_000003.10:g.98989616T>G NCBI36
NG_008119.1:g.28332T>G
NG_008119.2:g.28332T>G

Transcript Alleles

HGVS Amino-acid Change
NM_001278293.3:c.442T>G MANE Select NP_001265222.1:p.Cys148Gly
ENST00000463745.6:c.442T>G MANE Select ENSP00000419619.1:p.Cys148Gly
NM_001278293.1:c.442T>G NP_001265222.1:p.Cys148Gly
NM_001278293.2:c.442T>G NP_001265222.1:p.Cys148Gly
NM_001323513.1:c.442T>G NP_001310442.1:p.Cys148Gly
NM_001323513.2:c.442T>G NP_001310442.1:p.Cys148Gly
NM_001323514.1:c.442T>G NP_001310443.1:p.Cys148Gly
NM_001323514.2:c.442T>G NP_001310443.1:p.Cys148Gly
NM_032146.4:c.442T>G NP_115522.1:p.Cys148Gly
NM_032146.5:c.442T>G NP_115522.1:p.Cys148Gly
NM_177976.2:c.442T>G NP_816931.1:p.Cys148Gly
NM_177976.3:c.442T>G NP_816931.1:p.Cys148Gly
NR_103511.1:n.1025T>G
NR_103511.2:n.788T>G
NR_103511.3:n.788T>G
NR_136595.1:n.1025T>G
NR_136595.2:n.788T>G
NR_136597.1:n.926T>G
NR_136597.2:n.689T>G
NR_136598.1:n.930T>G
NR_136598.2:n.693T>G
NR_136600.1:n.926T>G
NR_136600.2:n.689T>G
NR_136600.3:n.689T>G
NR_136601.1:n.926T>G
NR_136601.2:n.689T>G
NR_136601.3:n.689T>G
NR_136602.1:n.926T>G
NR_136602.2:n.689T>G
NR_136602.3:n.689T>G
ENST00000335979.6:c.442T>G ENSP00000337722.2:p.Cys148Gly
ENST00000394206.5:c.442T>G ENSP00000377756.1:p.Cys148Gly
ENST00000462412.3:c.442T>G ENSP00000418740.2:p.Cys148Gly
ENST00000463745.5:c.442T>G ENSP00000419619.1:p.Cys148Gly
ENST00000476753.1:c.126T>G
ENST00000493990.5:c.442T>G ENSP00000418057.1:p.Cys148Gly
ENST00000496713.1:n.680T>G
ENST00000631834.1:c.304T>G ENSP00000488530.1:p.Cys102Gly
ENST00000631834.2:c.442T>G ENSP00000488530.2:p.Cys148Gly
XM_006713779.2:c.442T>G XP_006713842.1:p.Cys148Gly
XM_006713783.2:c.442T>G XP_006713846.1:p.Cys148Gly
XM_011513230.1:c.442T>G XP_011511532.1:p.Cys148Gly
XM_017007311.2:c.442T>G XP_016862800.1:p.Cys148Gly
XM_017007312.2:c.442T>G XP_016862801.1:p.Cys148Gly
XR_001740319.2:n.2866T>G
XR_001740321.2:n.2866T>G
XR_002959599.1:n.2925T>G
XR_924184.1:n.914T>G
XR_924184.3:n.2866T>G
XR_924185.1:n.1020T>G
XR_924185.3:n.2965T>G
XR_924186.1:n.1067T>G
XR_924186.3:n.3024T>G
XR_924187.1:n.914T>G
XR_924187.3:n.2866T>G
XR_924188.1:n.968T>G
XR_924188.3:n.2925T>G
XR_924189.1:n.914T>G
XR_924189.3:n.2866T>G