Canonical Allele Identifier: CA439956030

Gene: ART3 NUP54

Linked Data

• MyVariant Identifiers: chr4:g.77033627C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.76112474C>A , CM000666.2:g.76112474C>A	GRCh38
NC_000004.11:g.77033627C>A , CM000666.1:g.77033627C>A	GRCh37
NC_000004.10:g.77252651C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000511188.2:c.1158C>A (ART3)	ENSP00000422249.2:p.Ile386=
ENST00000695546.1:c.*1463G>T (NUP54)	ENSP00000512003.1:n.*1463G>T
ENST00000700440.1:c.1026C>A (ART3)	ENSP00000514989.1:p.Ile342=
ENST00000355810.9:c.1125C>A (ART3) MANE Select	ENSP00000348064.4:p.Ile375=
ENST00000341029.9:c.1059C>A (ART3)	ENSP00000343843.5:p.Ile353=
ENST00000349321.7:c.1092C>A (ART3)	ENSP00000304313.5:p.Ile364=
ENST00000355810.8:c.1125C>A (ART3)	ENSP00000348064.4:p.Ile375=
ENST00000395688.7:n.260C>A (ART3)
ENST00000504112.5:n.356C>A (ART3)
ENST00000506667.5:n.323C>A (ART3)
ENST00000510669.5:n.565C>A (ART3)
ENST00000510863.1:n.667C>A (ART3)
NM_001130016.2:c.1125C>A (ART3)	NP_001123488.1:p.Ile375=
NM_001130017.2:c.1059C>A (ART3)	NP_001123489.1:p.Ile353=
NM_001179.5:c.1092C>A (ART3)	NP_001170.2:p.Ile364=
XM_005262997.1:c.1158C>A (ART3)	XP_005263054.1:p.Ile386=
XM_005262999.1:c.1092C>A (ART3)	XP_005263056.1:p.Ile364=
XM_005263003.1:c.1029C>A (ART3)	XP_005263060.1:p.Ile343=
XM_005263004.1:c.1026C>A (ART3)	XP_005263061.1:p.Ile342=
XM_006714218.1:c.1128C>A (ART3)	XP_006714281.1:p.Ile376=
XM_006714220.1:c.1062C>A (ART3)	XP_006714283.1:p.Ile354=
XM_011531971.1:c.1062C>A (ART3)	XP_011530273.1:p.Ile354=
XM_017008210.2:c.1002C>A (ART3)	XP_016863699.1:p.Ile334=
XM_024454055.1:c.1158C>A (ART3)	XP_024309823.1:p.Ile386=
XM_024454056.1:c.1095C>A (ART3)	XP_024309824.1:p.Ile365=
XM_024454057.1:c.1092C>A (ART3)	XP_024309825.1:p.Ile364=
XM_024454058.1:c.1062C>A (ART3)	XP_024309826.1:p.Ile354=
XM_024454059.1:c.1062C>A (ART3)	XP_024309827.1:p.Ile354=
XM_024454060.1:c.1059C>A (ART3)	XP_024309828.1:p.Ile353=
XM_024454061.1:c.1029C>A (ART3)	XP_024309829.1:p.Ile343=
XM_024454062.1:c.1026C>A (ART3)	XP_024309830.1:p.Ile342=
XM_024454063.1:c.1026C>A (ART3)	XP_024309831.1:p.Ile342=
XR_002959732.1:n.2481C>A (ART3)
XR_002959733.1:n.2922C>A (ART3)
NM_001130016.3:c.1125C>A (ART3) MANE Select	NP_001123488.1:p.Ile375=
NM_001130017.3:c.1059C>A (ART3)	NP_001123489.1:p.Ile353=
NM_001179.6:c.1092C>A (ART3)	NP_001170.2:p.Ile364=
NM_001377173.1:c.1158C>A (ART3)	NP_001364102.1:p.Ile386=
NM_001377174.1:c.1092C>A (ART3)	NP_001364103.1:p.Ile364=
NM_001377175.1:c.1059C>A (ART3)	NP_001364104.1:p.Ile353=
NM_001377176.1:c.1029C>A (ART3)	NP_001364105.1:p.Ile343=
NM_001377177.1:c.996C>A (ART3)	NP_001364106.1:p.Ile332=
NM_001377178.1:c.996C>A (ART3)	NP_001364107.1:p.Ile332=
NM_001377179.1:c.996C>A (ART3)	NP_001364108.1:p.Ile332=
NM_001377180.1:c.963C>A (ART3)	NP_001364109.1:p.Ile321=
NM_001377181.1:c.936C>A (ART3)	NP_001364110.1:p.Ile312=
NM_001377182.1:c.936C>A (ART3)	NP_001364111.1:p.Ile312=
NM_001377183.1:c.903C>A (ART3)	NP_001364112.1:p.Ile301=
NM_001377184.1:c.903C>A (ART3)	NP_001364113.1:p.Ile301=
NM_001377185.1:c.870C>A (ART3)	NP_001364114.1:p.Ile290=