Canonical Allele Identifier: CA2346467522
Gene: ITPA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3213452A= , CM000682.2:g.3213452A= GRCh38
NC_000020.10:g.3194098A= , CM000682.1:g.3194098A= GRCh37
NC_000020.9:g.3142098A= NCBI36
NG_012093.1:g.9043A=
NG_012093.2:g.9586A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000380113.8:c.189+69A= MANE Select ENSP00000369456.3:n.189+69A=
ENST00000380113.7:c.189+69A= ENSP00000369456.3:n.189+69A=
ENST00000399838.3:c.67-533A= ENSP00000382732.3:n.67-533A=
ENST00000455664.6:c.138+69A= ENSP00000413282.1:n.138+69A=
ENST00000460550.5:n.163+226A=
ENST00000460676.5:n.302+26A=
ENST00000483354.5:n.224+226A=
ENST00000490838.6:n.173+69A=
ENST00000609835.5:n.243+69A=
NM_001267623.1:c.67-533A= NP_001254552.1:n.67-533A=
NM_033453.3:c.189+69A= NP_258412.1:n.189+69A=
NM_181493.2:c.138+69A= NP_852470.1:n.138+69A=
NR_052000.1:n.224+226A=
NR_052001.1:n.174+69A=
NR_052002.1:n.316+226A=
XM_006723564.2:c.189+69A= XP_006723627.1:n.189+69A=
XM_006723565.2:c.67-533A= XP_006723628.1:n.67-533A=
XM_011529234.1:c.189+69A= XP_011527536.1:n.189+69A=
XM_011529235.1:c.189+69A= XP_011527537.1:n.189+69A=
NM_001324236.1:c.-149+69A= NP_001311165.1:n.-149+69A=
NM_001324237.1:c.-149+69A= NP_001311166.1:n.-149+69A=
NM_001324238.1:c.-149+69A= NP_001311167.1:n.-149+69A=
NM_001324240.1:c.189+69A= NP_001311169.1:n.189+69A=
NM_001351739.1:c.-149+69A= NP_001338668.1:n.-149+69A=
NM_181493.3:c.138+69A= NP_852470.1:n.138+69A=
XM_006723564.3:c.189+69A= XP_006723627.1:n.189+69A=
XM_006723565.3:c.67-533A= XP_006723628.1:n.67-533A=
XM_011529234.2:c.189+69A= XP_011527536.1:n.189+69A=
XM_024451880.1:c.-681A= XP_024307648.1:n.-681A=
NM_033453.4:c.189+69A= MANE Select NP_258412.1:n.189+69A=
NM_001267623.2:c.67-533A= NP_001254552.1:n.67-533A=
NM_001324236.2:c.-149+69A= NP_001311165.1:n.-149+69A=
NM_001324237.2:c.-149+69A= NP_001311166.1:n.-149+69A=
NM_001324238.2:c.-149+69A= NP_001311167.1:n.-149+69A=
NM_001324240.2:c.189+69A= NP_001311169.1:n.189+69A=
NM_001351739.2:c.-149+69A= NP_001338668.1:n.-149+69A=
NM_181493.4:c.138+69A= NP_852470.1:n.138+69A=
NR_052000.2:n.416+226A=
NR_052002.2:n.178+226A=