Canonical Allele Identifier: CA11691348

Gene: ART3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.76101133C>G , CM000666.2:g.76101133C>G	GRCh38
NC_000004.11:g.77022286C>G , CM000666.1:g.77022286C>G	GRCh37
NC_000004.10:g.77241310C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000511188.2:c.937+114C>G	ENSP00000422249.2:n.937+114C>G
ENST00000700440.1:c.937+114C>G	ENSP00000514989.1:n.937+114C>G
ENST00000700441.1:c.907+309C>G	ENSP00000514990.1:n.907+309C>G
ENST00000355810.9:c.937+114C>G MANE Select	ENSP00000348064.4:n.937+114C>G
ENST00000341029.9:c.937+114C>G	ENSP00000343843.5:n.937+114C>G
ENST00000349321.7:c.937+114C>G	ENSP00000304313.5:n.937+114C>G
ENST00000355810.8:c.937+114C>G	ENSP00000348064.4:n.937+114C>G
ENST00000395688.7:n.138+114C>G
ENST00000504112.5:n.234+114C>G
ENST00000506313.1:n.160+114C>G
ENST00000506667.5:n.201+114C>G
ENST00000510669.5:n.355+114C>G
ENST00000511188.1:c.193+114C>G	ENSP00000422249.1:n.193+114C>G
NM_001130016.2:c.937+114C>G	NP_001123488.1:n.937+114C>G
NM_001130017.2:c.937+114C>G	NP_001123489.1:n.937+114C>G
NM_001179.5:c.937+114C>G	NP_001170.2:n.937+114C>G
XM_005262997.1:c.937+114C>G	XP_005263054.1:n.937+114C>G
XM_005262999.1:c.937+114C>G	XP_005263056.1:n.937+114C>G
XM_005263003.1:c.907+309C>G	XP_005263060.1:n.907+309C>G
XM_005263004.1:c.937+114C>G	XP_005263061.1:n.937+114C>G
XM_006714218.1:c.907+309C>G	XP_006714281.1:n.907+309C>G
XM_006714220.1:c.907+309C>G	XP_006714283.1:n.907+309C>G
XM_011531967.1:c.937+114C>G	XP_011530269.1:n.937+114C>G
XM_011531968.1:c.907+309C>G	XP_011530270.1:n.907+309C>G
XM_011531969.1:c.907+309C>G	XP_011530271.1:n.907+309C>G
XM_011531970.1:c.847+114C>G	XP_011530272.1:n.847+114C>G
XM_011531971.1:c.907+309C>G	XP_011530273.1:n.907+309C>G
XM_017008206.2:c.937+114C>G	XP_016863695.1:n.937+114C>G
XM_017008208.2:c.847+114C>G	XP_016863697.1:n.847+114C>G
XM_017008210.2:c.847+114C>G	XP_016863699.1:n.847+114C>G
XM_024454050.1:c.937+114C>G	XP_024309818.1:n.937+114C>G
XM_024454051.1:c.937+114C>G	XP_024309819.1:n.937+114C>G
XM_024454052.1:c.937+114C>G	XP_024309820.1:n.937+114C>G
XM_024454053.1:c.937+114C>G	XP_024309821.1:n.937+114C>G
XM_024454054.1:c.907+309C>G	XP_024309822.1:n.907+309C>G
XM_024454055.1:c.937+114C>G	XP_024309823.1:n.937+114C>G
XM_024454056.1:c.907+309C>G	XP_024309824.1:n.907+309C>G
XM_024454057.1:c.937+114C>G	XP_024309825.1:n.937+114C>G
XM_024454058.1:c.907+309C>G	XP_024309826.1:n.907+309C>G
XM_024454059.1:c.907+309C>G	XP_024309827.1:n.907+309C>G
XM_024454060.1:c.937+114C>G	XP_024309828.1:n.937+114C>G
XM_024454061.1:c.907+309C>G	XP_024309829.1:n.907+309C>G
XM_024454062.1:c.937+114C>G	XP_024309830.1:n.937+114C>G
XM_024454063.1:c.937+114C>G	XP_024309831.1:n.937+114C>G
XR_002959732.1:n.2359+114C>G
XR_002959733.1:n.2833+114C>G
NM_001130016.3:c.937+114C>G MANE Select	NP_001123488.1:n.937+114C>G
NM_001130017.3:c.937+114C>G	NP_001123489.1:n.937+114C>G
NM_001179.6:c.937+114C>G	NP_001170.2:n.937+114C>G
NM_001377173.1:c.937+114C>G	NP_001364102.1:n.937+114C>G
NM_001377174.1:c.937+114C>G	NP_001364103.1:n.937+114C>G
NM_001377175.1:c.937+114C>G	NP_001364104.1:n.937+114C>G
NM_001377176.1:c.907+114C>G	NP_001364105.1:n.907+114C>G
NM_001377177.1:c.907+114C>G	NP_001364106.1:n.907+114C>G
NM_001377178.1:c.907+114C>G	NP_001364107.1:n.907+114C>G
NM_001377179.1:c.841+114C>G	NP_001364108.1:n.841+114C>G
NM_001377180.1:c.841+114C>G	NP_001364109.1:n.841+114C>G
NM_001377181.1:c.847+2146C>G	NP_001364110.1:n.847+2146C>G
NM_001377182.1:c.847+2146C>G	NP_001364111.1:n.847+2146C>G
NM_001377183.1:c.814+3457C>G	NP_001364112.1:n.814+3457C>G
NM_001377184.1:c.814+3457C>G	NP_001364113.1:n.814+3457C>G
NM_001377185.1:c.782-11253C>G	NP_001364114.1:n.782-11253C>G