Canonical Allele Identifier: CA2346467526
Gene: ITPA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3213462G= , CM000682.2:g.3213462G= GRCh38
NC_000020.10:g.3194108G= , CM000682.1:g.3194108G= GRCh37
NC_000020.9:g.3142108G= NCBI36
NG_012093.1:g.9053G=
NG_012093.2:g.9596G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000380113.8:c.189+79G= MANE Select ENSP00000369456.3:n.189+79G=
ENST00000380113.7:c.189+79G= ENSP00000369456.3:n.189+79G=
ENST00000399838.3:c.67-523G= ENSP00000382732.3:n.67-523G=
ENST00000455664.6:c.138+79G= ENSP00000413282.1:n.138+79G=
ENST00000460550.5:n.163+236G=
ENST00000460676.5:n.302+36G=
ENST00000483354.5:n.224+236G=
ENST00000490838.6:n.173+79G=
ENST00000609835.5:n.243+79G=
NM_001267623.1:c.67-523G= NP_001254552.1:n.67-523G=
NM_033453.3:c.189+79G= NP_258412.1:n.189+79G=
NM_181493.2:c.138+79G= NP_852470.1:n.138+79G=
NR_052000.1:n.224+236G=
NR_052001.1:n.174+79G=
NR_052002.1:n.316+236G=
XM_006723564.2:c.189+79G= XP_006723627.1:n.189+79G=
XM_006723565.2:c.67-523G= XP_006723628.1:n.67-523G=
XM_011529234.1:c.189+79G= XP_011527536.1:n.189+79G=
XM_011529235.1:c.189+79G= XP_011527537.1:n.189+79G=
NM_001324236.1:c.-149+79G= NP_001311165.1:n.-149+79G=
NM_001324237.1:c.-149+79G= NP_001311166.1:n.-149+79G=
NM_001324238.1:c.-149+79G= NP_001311167.1:n.-149+79G=
NM_001324240.1:c.189+79G= NP_001311169.1:n.189+79G=
NM_001351739.1:c.-149+79G= NP_001338668.1:n.-149+79G=
NM_181493.3:c.138+79G= NP_852470.1:n.138+79G=
XM_006723564.3:c.189+79G= XP_006723627.1:n.189+79G=
XM_006723565.3:c.67-523G= XP_006723628.1:n.67-523G=
XM_011529234.2:c.189+79G= XP_011527536.1:n.189+79G=
XM_024451880.1:c.-671G= XP_024307648.1:n.-671G=
NM_033453.4:c.189+79G= MANE Select NP_258412.1:n.189+79G=
NM_001267623.2:c.67-523G= NP_001254552.1:n.67-523G=
NM_001324236.2:c.-149+79G= NP_001311165.1:n.-149+79G=
NM_001324237.2:c.-149+79G= NP_001311166.1:n.-149+79G=
NM_001324238.2:c.-149+79G= NP_001311167.1:n.-149+79G=
NM_001324240.2:c.189+79G= NP_001311169.1:n.189+79G=
NM_001351739.2:c.-149+79G= NP_001338668.1:n.-149+79G=
NM_181493.4:c.138+79G= NP_852470.1:n.138+79G=
NR_052000.2:n.416+236G=
NR_052002.2:n.178+236G=