Canonical Allele Identifier: CA353587022
Community Standard Title: NM_001278293.3(ARL6):c.262C>T (p.Gln88Ter)
Gene: ARL6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.97784962C>T , CM000665.2:g.97784962C>T GRCh38
NC_000003.11:g.97503806C>T , CM000665.1:g.97503806C>T GRCh37
NC_000003.10:g.98986496C>T NCBI36
NG_008119.1:g.25212C>T
NG_008119.2:g.25212C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001278293.3:c.262C>T MANE Select NP_001265222.1:p.Gln88Ter
ENST00000463745.6:c.262C>T MANE Select ENSP00000419619.1:p.Gln88Ter
NM_001278293.1:c.262C>T NP_001265222.1:p.Gln88Ter
NM_001278293.2:c.262C>T NP_001265222.1:p.Gln88Ter
NM_001323513.1:c.262C>T NP_001310442.1:p.Gln88Ter
NM_001323513.2:c.262C>T NP_001310442.1:p.Gln88Ter
NM_001323514.1:c.262C>T NP_001310443.1:p.Gln88Ter
NM_001323514.2:c.262C>T NP_001310443.1:p.Gln88Ter
NM_032146.4:c.262C>T NP_115522.1:p.Gln88Ter
NM_032146.5:c.262C>T NP_115522.1:p.Gln88Ter
NM_177976.2:c.262C>T NP_816931.1:p.Gln88Ter
NM_177976.3:c.262C>T NP_816931.1:p.Gln88Ter
NR_103511.1:n.845C>T
NR_103511.2:n.608C>T
NR_103511.3:n.608C>T
NR_136595.1:n.845C>T
NR_136595.2:n.608C>T
NR_136597.1:n.746C>T
NR_136597.2:n.509C>T
NR_136598.1:n.750C>T
NR_136598.2:n.513C>T
NR_136600.1:n.746C>T
NR_136600.2:n.509C>T
NR_136600.3:n.509C>T
NR_136601.1:n.746C>T
NR_136601.2:n.509C>T
NR_136601.3:n.509C>T
NR_136602.1:n.746C>T
NR_136602.2:n.509C>T
NR_136602.3:n.509C>T
ENST00000335979.6:c.262C>T ENSP00000337722.2:p.Gln88Ter
ENST00000394206.5:c.262C>T ENSP00000377756.1:p.Gln88Ter
ENST00000462412.2:c.262C>T ENSP00000418740.1:p.Gln88Ter
ENST00000462412.3:c.262C>T ENSP00000418740.2:p.Gln88Ter
ENST00000463745.5:c.262C>T ENSP00000419619.1:p.Gln88Ter
ENST00000493990.5:c.262C>T ENSP00000418057.1:p.Gln88Ter
ENST00000496713.1:n.500C>T
ENST00000631834.1:c.124C>T ENSP00000488530.1:p.Gln42Ter
ENST00000631834.2:c.262C>T ENSP00000488530.2:p.Gln88Ter
XM_006713779.2:c.262C>T XP_006713842.1:p.Gln88Ter
XM_006713783.2:c.262C>T XP_006713846.1:p.Gln88Ter
XM_011513230.1:c.262C>T XP_011511532.1:p.Gln88Ter
XM_017007311.2:c.262C>T XP_016862800.1:p.Gln88Ter
XM_017007312.2:c.262C>T XP_016862801.1:p.Gln88Ter
XR_001740319.2:n.2686C>T
XR_001740321.2:n.2686C>T
XR_002959599.1:n.2745C>T
XR_924184.1:n.734C>T
XR_924184.3:n.2686C>T
XR_924185.1:n.840C>T
XR_924185.3:n.2785C>T
XR_924186.1:n.887C>T
XR_924186.3:n.2844C>T
XR_924187.1:n.734C>T
XR_924187.3:n.2686C>T
XR_924188.1:n.788C>T
XR_924188.3:n.2745C>T
XR_924189.1:n.734C>T
XR_924189.3:n.2686C>T