Canonical Allele Identifier: CA353586338

Gene: ARL6

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.97780681T>G , CM000665.2:g.97780681T>G	GRCh38
NC_000003.11:g.97499525T>G , CM000665.1:g.97499525T>G	GRCh37
NC_000003.10:g.98982215T>G	NCBI36
NG_008119.1:g.20931T>G
NG_008119.2:g.20931T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001278293.3:c.252T>G MANE Select	NP_001265222.1:p.Tyr84Ter
ENST00000463745.6:c.252T>G MANE Select	ENSP00000419619.1:p.Tyr84Ter
NM_001278293.1:c.252T>G	NP_001265222.1:p.Tyr84Ter
NM_001278293.2:c.252T>G	NP_001265222.1:p.Tyr84Ter
NM_001323513.1:c.252T>G	NP_001310442.1:p.Tyr84Ter
NM_001323513.2:c.252T>G	NP_001310442.1:p.Tyr84Ter
NM_001323514.1:c.252T>G	NP_001310443.1:p.Tyr84Ter
NM_001323514.2:c.252T>G	NP_001310443.1:p.Tyr84Ter
NM_032146.4:c.252T>G	NP_115522.1:p.Tyr84Ter
NM_032146.5:c.252T>G	NP_115522.1:p.Tyr84Ter
NM_177976.2:c.252T>G	NP_816931.1:p.Tyr84Ter
NM_177976.3:c.252T>G	NP_816931.1:p.Tyr84Ter
NR_103511.1:n.835T>G
NR_103511.2:n.598T>G
NR_103511.3:n.598T>G
NR_136595.1:n.835T>G
NR_136595.2:n.598T>G
NR_136597.1:n.736T>G
NR_136597.2:n.499T>G
NR_136598.1:n.736T>G
NR_136598.2:n.499T>G
NR_136600.1:n.736T>G
NR_136600.2:n.499T>G
NR_136600.3:n.499T>G
NR_136601.1:n.736T>G
NR_136601.2:n.499T>G
NR_136601.3:n.499T>G
NR_136602.1:n.736T>G
NR_136602.2:n.499T>G
NR_136602.3:n.499T>G
ENST00000335979.6:c.252T>G	ENSP00000337722.2:p.Tyr84Ter
ENST00000394206.5:c.252T>G	ENSP00000377756.1:p.Tyr84Ter
ENST00000462412.2:c.252T>G	ENSP00000418740.1:p.Tyr84Ter
ENST00000462412.3:c.252T>G	ENSP00000418740.2:p.Tyr84Ter
ENST00000463745.5:c.252T>G	ENSP00000419619.1:p.Tyr84Ter
ENST00000493990.5:c.252T>G	ENSP00000418057.1:p.Tyr84Ter
ENST00000496713.1:n.490T>G
ENST00000631834.1:c.114T>G	ENSP00000488530.1:p.Tyr38Ter
ENST00000631834.2:c.252T>G	ENSP00000488530.2:p.Tyr84Ter
XM_006713779.2:c.252T>G	XP_006713842.1:p.Tyr84Ter
XM_006713783.2:c.252T>G	XP_006713846.1:p.Tyr84Ter
XM_011513230.1:c.252T>G	XP_011511532.1:p.Tyr84Ter
XM_017007311.2:c.252T>G	XP_016862800.1:p.Tyr84Ter
XM_017007312.2:c.252T>G	XP_016862801.1:p.Tyr84Ter
XR_001740319.2:n.2676T>G
XR_001740321.2:n.2676T>G
XR_002959599.1:n.2735T>G
XR_924184.1:n.724T>G
XR_924184.3:n.2676T>G
XR_924185.1:n.830T>G
XR_924185.3:n.2775T>G
XR_924186.1:n.877T>G
XR_924186.3:n.2834T>G
XR_924187.1:n.724T>G
XR_924187.3:n.2676T>G
XR_924188.1:n.778T>G
XR_924188.3:n.2735T>G
XR_924189.1:n.724T>G
XR_924189.3:n.2676T>G