Canonical Allele Identifier: CA79492192

Gene: ARL6

Linked Data

• ClinVar Variation Id: 1582768
• ClinVar RCV Id: RCV002097582
• dbSNP Id: rs888140182
• MyVariant Identifiers: chr3:g.97499522T>C (hg19) ; chr3:g.97780678T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.97780678T>C , CM000665.2:g.97780678T>C	GRCh38
NC_000003.11:g.97499522T>C , CM000665.1:g.97499522T>C	GRCh37
NC_000003.10:g.98982212T>C	NCBI36
NG_008119.1:g.20928T>C
NG_008119.2:g.20928T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000462412.3:c.249T>C	ENSP00000418740.2:p.Tyr83=
ENST00000631834.2:c.249T>C	ENSP00000488530.2:p.Tyr83=
ENST00000463745.6:c.249T>C MANE Select	ENSP00000419619.1:p.Tyr83=
ENST00000335979.6:c.249T>C	ENSP00000337722.2:p.Tyr83=
ENST00000394206.5:c.249T>C	ENSP00000377756.1:p.Tyr83=
ENST00000462412.2:c.249T>C	ENSP00000418740.1:p.Tyr83=
ENST00000463745.5:c.249T>C	ENSP00000419619.1:p.Tyr83=
ENST00000493990.5:c.249T>C	ENSP00000418057.1:p.Tyr83=
ENST00000496713.1:n.487T>C
ENST00000631834.1:c.111T>C	ENSP00000488530.1:p.Tyr37=
NM_001278293.1:c.249T>C	NP_001265222.1:p.Tyr83=
NM_032146.4:c.249T>C	NP_115522.1:p.Tyr83=
NM_177976.2:c.249T>C	NP_816931.1:p.Tyr83=
NR_103511.1:n.832T>C
XM_006713779.2:c.249T>C	XP_006713842.1:p.Tyr83=
XM_006713783.2:c.249T>C	XP_006713846.1:p.Tyr83=
XM_011513230.1:c.249T>C	XP_011511532.1:p.Tyr83=
XR_924184.1:n.721T>C
XR_924185.1:n.827T>C
XR_924186.1:n.874T>C
XR_924187.1:n.721T>C
XR_924188.1:n.775T>C
XR_924189.1:n.721T>C
NM_001278293.2:c.249T>C	NP_001265222.1:p.Tyr83=
NM_001323513.1:c.249T>C	NP_001310442.1:p.Tyr83=
NM_001323514.1:c.249T>C	NP_001310443.1:p.Tyr83=
NM_032146.5:c.249T>C	NP_115522.1:p.Tyr83=
NM_177976.3:c.249T>C	NP_816931.1:p.Tyr83=
NR_136595.1:n.832T>C
NR_136597.1:n.733T>C
NR_136598.1:n.733T>C
NR_136600.1:n.733T>C
NR_136601.1:n.733T>C
NR_136602.1:n.733T>C
XM_017007311.2:c.249T>C	XP_016862800.1:p.Tyr83=
XM_017007312.2:c.249T>C	XP_016862801.1:p.Tyr83=
XR_001740319.2:n.2673T>C
XR_001740321.2:n.2673T>C
XR_002959599.1:n.2732T>C
XR_924184.3:n.2673T>C
XR_924185.3:n.2772T>C
XR_924186.3:n.2831T>C
XR_924187.3:n.2673T>C
XR_924188.3:n.2732T>C
XR_924189.3:n.2673T>C
NM_001278293.3:c.249T>C MANE Select	NP_001265222.1:p.Tyr83=
NM_001323513.2:c.249T>C	NP_001310442.1:p.Tyr83=
NM_001323514.2:c.249T>C	NP_001310443.1:p.Tyr83=
NR_103511.2:n.595T>C
NR_136595.2:n.595T>C
NR_136597.2:n.496T>C
NR_136598.2:n.496T>C
NR_136600.2:n.496T>C
NR_136601.2:n.496T>C
NR_136602.2:n.496T>C
NR_103511.3:n.595T>C
NR_136600.3:n.496T>C
NR_136601.3:n.496T>C
NR_136602.3:n.496T>C