Canonical Allele Identifier: CA463512337

Gene: NAPRT

Linked Data

• MyVariant Identifiers: chr8:g.144657636C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143575466C>G , CM000670.2:g.143575466C>G	GRCh38
NC_000008.10:g.144657636C>G , CM000670.1:g.144657636C>G	GRCh37
NC_000008.9:g.144728779C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449291.7:c.1248G>C MANE Select	ENSP00000401508.2:p.Thr416=
ENST00000340490.7:c.1248G>C	ENSP00000341136.3:p.Thr416=
ENST00000426292.7:c.1248G>C	ENSP00000390949.3:p.Thr416=
ENST00000435154.7:c.1248G>C	ENSP00000405670.3:p.Thr416=
ENST00000449291.6:c.1248G>C	ENSP00000401508.2:p.Thr416=
ENST00000460623.5:c.226G>C
ENST00000464332.5:n.792G>C
ENST00000525583.5:c.1032G>C
NM_001286829.1:c.1248G>C	NP_001273758.1:p.Thr416=
NM_145201.5:c.1248G>C	NP_660202.3:p.Thr416=
XM_011517377.1:c.1248G>C	XP_011515679.1:p.Thr416=
NM_001363145.1:c.1167G>C	NP_001350074.1:p.Thr389=
NM_001363146.1:c.564G>C	NP_001350075.1:p.Thr188=
XM_017013975.2:c.1467G>C	XP_016869464.1:p.Thr489=
XM_017013976.2:c.1467G>C	XP_016869465.1:p.Thr489=
XM_017013977.2:c.1167G>C	XP_016869466.1:p.Thr389=
XM_017013978.2:c.1467G>C	XP_016869467.1:p.Thr489=
XM_017013979.2:c.564G>C	XP_016869468.1:p.Thr188=
XM_024447332.1:c.885G>C	XP_024303100.1:p.Thr295=
XM_024447333.1:c.483G>C	XP_024303101.1:p.Thr161=
NM_145201.6:c.1248G>C MANE Select	NP_660202.3:p.Thr416=
NM_001286829.2:c.1248G>C	NP_001273758.1:p.Thr416=