Canonical Allele Identifier: CA79493980

Gene: ARL6

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.97788126T>C , CM000665.2:g.97788126T>C	GRCh38
NC_000003.11:g.97506970T>C , CM000665.1:g.97506970T>C	GRCh37
NC_000003.10:g.98989660T>C	NCBI36
NG_008119.1:g.28376T>C
NG_008119.2:g.28376T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001278293.3:c.479+7T>C MANE Select	NP_001265222.1:n.479+7T>C
ENST00000463745.6:c.479+7T>C MANE Select	ENSP00000419619.1:n.479+7T>C
NM_001278293.1:c.479+7T>C	NP_001265222.1:n.479+7T>C
NM_001278293.2:c.479+7T>C	NP_001265222.1:n.479+7T>C
NM_001323513.1:c.479+7T>C	NP_001310442.1:n.479+7T>C
NM_001323513.2:c.479+7T>C	NP_001310442.1:n.479+7T>C
NM_001323514.1:c.479+7T>C	NP_001310443.1:n.479+7T>C
NM_001323514.2:c.479+7T>C	NP_001310443.1:n.479+7T>C
NM_032146.4:c.479+7T>C	NP_115522.1:n.479+7T>C
NM_032146.5:c.479+7T>C	NP_115522.1:n.479+7T>C
NM_177976.2:c.479+7T>C	NP_816931.1:n.479+7T>C
NM_177976.3:c.479+7T>C	NP_816931.1:n.479+7T>C
NR_103511.1:n.1062+7T>C
NR_103511.2:n.825+7T>C
NR_103511.3:n.825+7T>C
NR_136595.1:n.1062+7T>C
NR_136595.2:n.825+7T>C
NR_136597.1:n.963+7T>C
NR_136597.2:n.726+7T>C
NR_136598.1:n.967+7T>C
NR_136598.2:n.730+7T>C
NR_136600.1:n.963+7T>C
NR_136600.2:n.726+7T>C
NR_136600.3:n.726+7T>C
NR_136601.1:n.963+7T>C
NR_136601.2:n.726+7T>C
NR_136601.3:n.726+7T>C
NR_136602.1:n.963+7T>C
NR_136602.2:n.726+7T>C
NR_136602.3:n.726+7T>C
ENST00000335979.6:c.479+7T>C	ENSP00000337722.2:n.479+7T>C
ENST00000394206.5:c.479+7T>C	ENSP00000377756.1:n.479+7T>C
ENST00000462412.3:c.479+7T>C	ENSP00000418740.2:n.479+7T>C
ENST00000463745.5:c.479+7T>C	ENSP00000419619.1:n.479+7T>C
ENST00000476753.1:c.163+7T>C
ENST00000493990.5:c.479+7T>C	ENSP00000418057.1:n.479+7T>C
ENST00000496713.1:n.717+7T>C
ENST00000631834.1:c.341+7T>C	ENSP00000488530.1:n.341+7T>C
ENST00000631834.2:c.479+7T>C	ENSP00000488530.2:n.479+7T>C
XM_006713779.2:c.479+7T>C	XP_006713842.1:n.479+7T>C
XM_006713783.2:c.479+7T>C	XP_006713846.1:n.479+7T>C
XM_011513230.1:c.479+7T>C	XP_011511532.1:n.479+7T>C
XM_017007311.2:c.479+7T>C	XP_016862800.1:n.479+7T>C
XM_017007312.2:c.479+7T>C	XP_016862801.1:n.479+7T>C
XR_001740319.2:n.2903+7T>C
XR_001740321.2:n.2903+7T>C
XR_002959599.1:n.2962+7T>C
XR_924184.1:n.951+7T>C
XR_924184.3:n.2903+7T>C
XR_924185.1:n.1057+7T>C
XR_924185.3:n.3002+7T>C
XR_924186.1:n.1104+7T>C
XR_924186.3:n.3061+7T>C
XR_924187.1:n.951+7T>C
XR_924187.3:n.2903+7T>C
XR_924188.1:n.1005+7T>C
XR_924188.3:n.2962+7T>C
XR_924189.1:n.951+7T>C
XR_924189.3:n.2903+7T>C