Canonical Allele Identifier: CA2263863500
Community Standard Title: NM_002204.4(ITGA3):c.2155G= (p.Ala719=)
Gene: ITGA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50078061G= , CM000679.2:g.50078061G= GRCh38
NC_000017.10:g.48155425G= , CM000679.1:g.48155425G= GRCh37
NC_000017.9:g.45510424G= NCBI36
NG_029107.2:g.27086G=

Transcript Alleles

HGVS Amino-acid Change
NM_002204.4:c.2155G= MANE Select NP_002195.1:p.Ala719=
ENST00000320031.13:c.2155G= MANE Select ENSP00000315190.8:p.Ala719=
NM_002204.2:c.2155G= NP_002195.1:p.Ala719=
NM_002204.3:c.2155G= NP_002195.1:p.Ala719=
NM_005501.2:c.2155G= NP_005492.1:p.Ala719=
ENST00000007722.11:c.2155G= ENSP00000007722.7:p.Ala719=
ENST00000320031.12:c.2155G= ENSP00000315190.8:p.Ala719=
ENST00000505306.5:n.3076G=
ENST00000506827.1:c.290G=
ENST00000507771.5:n.64G=
ENST00000515147.1:n.58G=
XM_005257308.1:c.1750G= XP_005257365.1:p.Ala584=
XM_005257308.2:c.1750G= XP_005257365.1:p.Ala584=
XR_001752507.1:n.2571G=