Canonical Allele Identifier: CA1825861477

Gene: NAPRT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143575487G= , CM000670.2:g.143575487G=	GRCh38
NC_000008.10:g.144657657G= , CM000670.1:g.144657657G=	GRCh37
NC_000008.9:g.144728800G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449291.7:c.1227C= MANE Select	ENSP00000401508.2:p.Thr409=
ENST00000340490.7:c.1227C=	ENSP00000341136.3:p.Thr409=
ENST00000426292.7:c.1227C=	ENSP00000390949.3:p.Thr409=
ENST00000435154.7:c.1227C=	ENSP00000405670.3:p.Thr409=
ENST00000449291.6:c.1227C=	ENSP00000401508.2:p.Thr409=
ENST00000460623.5:c.205C=
ENST00000464332.5:n.771C=
ENST00000525583.5:c.1011C=
NM_001286829.1:c.1227C=	NP_001273758.1:p.Thr409=
NM_145201.5:c.1227C=	NP_660202.3:p.Thr409=
XM_011517377.1:c.1227C=	XP_011515679.1:p.Thr409=
NM_001363145.1:c.1146C=	NP_001350074.1:p.Thr382=
NM_001363146.1:c.543C=	NP_001350075.1:p.Thr181=
XM_017013975.2:c.1446C=	XP_016869464.1:p.Thr482=
XM_017013976.2:c.1446C=	XP_016869465.1:p.Thr482=
XM_017013977.2:c.1146C=	XP_016869466.1:p.Thr382=
XM_017013978.2:c.1446C=	XP_016869467.1:p.Thr482=
XM_017013979.2:c.543C=	XP_016869468.1:p.Thr181=
XM_024447332.1:c.864C=	XP_024303100.1:p.Thr288=
XM_024447333.1:c.462C=	XP_024303101.1:p.Thr154=
NM_145201.6:c.1227C= MANE Select	NP_660202.3:p.Thr409=
NM_001286829.2:c.1227C=	NP_001273758.1:p.Thr409=