Canonical Allele Identifier: CA372448522

Gene: NAPRT

Linked Data

• MyVariant Identifiers: chr8:g.144657042A>C (hg19) ; chr8:g.143574872A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143574872A>C , CM000670.2:g.143574872A>C	GRCh38
NC_000008.10:g.144657042A>C , CM000670.1:g.144657042A>C	GRCh37
NC_000008.9:g.144728185A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449291.7:c.1583T>G MANE Select	ENSP00000401508.2:p.Leu528Arg
ENST00000340490.7:c.1668T>G	ENSP00000341136.3:p.Pro556=
ENST00000426292.7:c.1544T>G	ENSP00000390949.3:p.Leu515Arg
ENST00000435154.7:c.*292T>G	ENSP00000405670.3:n.*292T>G
ENST00000449291.6:c.1583T>G	ENSP00000401508.2:p.Leu528Arg
ENST00000460623.5:c.607T>G
ENST00000464332.5:n.1127T>G
ENST00000498076.5:n.362T>G
ENST00000529179.1:n.367T>G
NM_001286829.1:c.1544T>G	NP_001273758.1:p.Leu515Arg
NM_145201.5:c.1583T>G	NP_660202.3:p.Leu528Arg
XM_011517377.1:c.1320T>G	XP_011515679.1:p.Pro440=
NM_001363145.1:c.1502T>G	NP_001350074.1:p.Leu501Arg
NM_001363146.1:c.899T>G	NP_001350075.1:p.Leu300Arg
XM_017013975.2:c.1887T>G	XP_016869464.1:p.Pro629=
XM_017013976.2:c.1802T>G	XP_016869465.1:p.Leu601Arg
XM_017013977.2:c.1587T>G	XP_016869466.1:p.Pro529=
XM_017013978.2:c.1539T>G	XP_016869467.1:p.Pro513=
XM_017013979.2:c.984T>G	XP_016869468.1:p.Pro328=
XM_024447332.1:c.957T>G	XP_024303100.1:p.Pro319=
XM_024447333.1:c.903T>G	XP_024303101.1:p.Pro301=
NM_145201.6:c.1583T>G MANE Select	NP_660202.3:p.Leu528Arg
NM_001286829.2:c.1544T>G	NP_001273758.1:p.Leu515Arg