Canonical Allele Identifier: CA2346467556

Gene: ITPA

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3213515T= , CM000682.2:g.3213515T=	GRCh38
NC_000020.10:g.3194161T= , CM000682.1:g.3194161T=	GRCh37
NC_000020.9:g.3142161T=	NCBI36
NG_012093.1:g.9106T=
NG_012093.2:g.9649T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380113.8:c.189+132T= MANE Select	ENSP00000369456.3:n.189+132T=
ENST00000380113.7:c.189+132T=	ENSP00000369456.3:n.189+132T=
ENST00000399838.3:c.67-470T=	ENSP00000382732.3:n.67-470T=
ENST00000455664.6:c.138+132T=	ENSP00000413282.1:n.138+132T=
ENST00000460550.5:n.163+289T=
ENST00000460676.5:n.302+89T=
ENST00000483354.5:n.224+289T=
ENST00000490838.6:n.173+132T=
ENST00000609835.5:n.243+132T=
NM_001267623.1:c.67-470T=	NP_001254552.1:n.67-470T=
NM_033453.3:c.189+132T=	NP_258412.1:n.189+132T=
NM_181493.2:c.138+132T=	NP_852470.1:n.138+132T=
NR_052000.1:n.224+289T=
NR_052001.1:n.174+132T=
NR_052002.1:n.316+289T=
XM_006723564.2:c.189+132T=	XP_006723627.1:n.189+132T=
XM_006723565.2:c.67-470T=	XP_006723628.1:n.67-470T=
XM_011529234.1:c.189+132T=	XP_011527536.1:n.189+132T=
XM_011529235.1:c.189+132T=	XP_011527537.1:n.189+132T=
NM_001324236.1:c.-149+132T=	NP_001311165.1:n.-149+132T=
NM_001324237.1:c.-149+132T=	NP_001311166.1:n.-149+132T=
NM_001324238.1:c.-149+132T=	NP_001311167.1:n.-149+132T=
NM_001324240.1:c.189+132T=	NP_001311169.1:n.189+132T=
NM_001351739.1:c.-149+132T=	NP_001338668.1:n.-149+132T=
NM_181493.3:c.138+132T=	NP_852470.1:n.138+132T=
XM_006723564.3:c.189+132T=	XP_006723627.1:n.189+132T=
XM_006723565.3:c.67-470T=	XP_006723628.1:n.67-470T=
XM_011529234.2:c.189+132T=	XP_011527536.1:n.189+132T=
XM_024451880.1:c.-618T=	XP_024307648.1:n.-618T=
NM_033453.4:c.189+132T= MANE Select	NP_258412.1:n.189+132T=
NM_001267623.2:c.67-470T=	NP_001254552.1:n.67-470T=
NM_001324236.2:c.-149+132T=	NP_001311165.1:n.-149+132T=
NM_001324237.2:c.-149+132T=	NP_001311166.1:n.-149+132T=
NM_001324238.2:c.-149+132T=	NP_001311167.1:n.-149+132T=
NM_001324240.2:c.189+132T=	NP_001311169.1:n.189+132T=
NM_001351739.2:c.-149+132T=	NP_001338668.1:n.-149+132T=
NM_181493.4:c.138+132T=	NP_852470.1:n.138+132T=
NR_052000.2:n.416+289T=
NR_052002.2:n.178+289T=