Canonical Allele Identifier: CA353582837

Gene: ARL6

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.97768231G>A , CM000665.2:g.97768231G>A	GRCh38
NC_000003.11:g.97487075G>A , CM000665.1:g.97487075G>A	GRCh37
NC_000003.10:g.98969765G>A	NCBI36
NG_008119.1:g.8481G>A
NG_008119.2:g.8481G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001278293.3:c.123+1G>A MANE Select	NP_001265222.1:n.123+1G>A
ENST00000463745.6:c.123+1G>A MANE Select	ENSP00000419619.1:n.123+1G>A
NM_001278293.1:c.123+1G>A	NP_001265222.1:n.123+1G>A
NM_001278293.2:c.123+1G>A	NP_001265222.1:n.123+1G>A
NM_001323513.1:c.123+1G>A	NP_001310442.1:n.123+1G>A
NM_001323513.2:c.123+1G>A	NP_001310442.1:n.123+1G>A
NM_001323514.1:c.123+1G>A	NP_001310443.1:n.123+1G>A
NM_001323514.2:c.123+1G>A	NP_001310443.1:n.123+1G>A
NM_032146.4:c.123+1G>A	NP_115522.1:n.123+1G>A
NM_032146.5:c.123+1G>A	NP_115522.1:n.123+1G>A
NM_177976.2:c.123+1G>A	NP_816931.1:n.123+1G>A
NM_177976.3:c.123+1G>A	NP_816931.1:n.123+1G>A
NR_103511.1:n.706+1G>A
NR_103511.2:n.469+1G>A
NR_103511.3:n.469+1G>A
NR_136595.1:n.706+1G>A
NR_136595.2:n.469+1G>A
NR_136597.1:n.607+1G>A
NR_136597.2:n.370+1G>A
NR_136598.1:n.607+1G>A
NR_136598.2:n.370+1G>A
NR_136600.1:n.607+1G>A
NR_136600.2:n.370+1G>A
NR_136600.3:n.370+1G>A
NR_136601.1:n.607+1G>A
NR_136601.2:n.370+1G>A
NR_136601.3:n.370+1G>A
NR_136602.1:n.607+1G>A
NR_136602.2:n.370+1G>A
NR_136602.3:n.370+1G>A
ENST00000335979.6:c.123+1G>A	ENSP00000337722.2:n.123+1G>A
ENST00000394206.5:c.123+1G>A	ENSP00000377756.1:n.123+1G>A
ENST00000462412.2:c.123+1G>A	ENSP00000418740.1:n.123+1G>A
ENST00000462412.3:c.123+1G>A	ENSP00000418740.2:n.123+1G>A
ENST00000463745.5:c.123+1G>A	ENSP00000419619.1:n.123+1G>A
ENST00000493990.5:c.123+1G>A	ENSP00000418057.1:n.123+1G>A
ENST00000496713.1:n.361+1G>A
ENST00000631834.2:c.123+1G>A	ENSP00000488530.2:n.123+1G>A
XM_006713779.2:c.123+1G>A	XP_006713842.1:n.123+1G>A
XM_006713783.2:c.123+1G>A	XP_006713846.1:n.123+1G>A
XM_011513230.1:c.123+1G>A	XP_011511532.1:n.123+1G>A
XM_017007311.2:c.123+1G>A	XP_016862800.1:n.123+1G>A
XM_017007312.2:c.123+1G>A	XP_016862801.1:n.123+1G>A
XR_001740319.2:n.2547+1G>A
XR_001740321.2:n.2547+1G>A
XR_002959599.1:n.2606+1G>A
XR_924184.1:n.595+1G>A
XR_924184.3:n.2547+1G>A
XR_924185.1:n.701+1G>A
XR_924185.3:n.2646+1G>A
XR_924186.1:n.748+1G>A
XR_924186.3:n.2705+1G>A
XR_924187.1:n.595+1G>A
XR_924187.3:n.2547+1G>A
XR_924188.1:n.649+1G>A
XR_924188.3:n.2606+1G>A
XR_924189.1:n.595+1G>A
XR_924189.3:n.2547+1G>A