Canonical Allele Identifier: CA187547938

Gene: NAPRT

Linked Data

• dbSNP Id: rs376795388
• gnomAD v2: 8-144657678-G-T
• gnomAD v3: 8-143575508-G-T
• gnomAD v4: 8-143575508-G-T
• MyVariant Identifiers: chr8:g.144657678G>T (hg19) ; chr8:g.144657678_144657679delinsTC (hg19) ; chr8:g.143575508G>T (hg38) ; chr8:g.143575508_143575509delinsTC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143575508G>T , CM000670.2:g.143575508G>T	GRCh38
NC_000008.10:g.144657678G>T , CM000670.1:g.144657678G>T	GRCh37
NC_000008.9:g.144728821G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449291.7:c.1206C>A MANE Select	ENSP00000401508.2:p.Gly402=
ENST00000340490.7:c.1206C>A	ENSP00000341136.3:p.Gly402=
ENST00000426292.7:c.1206C>A	ENSP00000390949.3:p.Gly402=
ENST00000435154.7:c.1206C>A	ENSP00000405670.3:p.Gly402=
ENST00000449291.6:c.1206C>A	ENSP00000401508.2:p.Gly402=
ENST00000460623.5:c.184C>A
ENST00000464332.5:n.750C>A
ENST00000525583.5:c.990C>A
NM_001286829.1:c.1206C>A	NP_001273758.1:p.Gly402=
NM_145201.5:c.1206C>A	NP_660202.3:p.Gly402=
XM_011517377.1:c.1206C>A	XP_011515679.1:p.Gly402=
NM_001363145.1:c.1125C>A	NP_001350074.1:p.Gly375=
NM_001363146.1:c.522C>A	NP_001350075.1:p.Gly174=
XM_017013975.2:c.1425C>A	XP_016869464.1:p.Gly475=
XM_017013976.2:c.1425C>A	XP_016869465.1:p.Gly475=
XM_017013977.2:c.1125C>A	XP_016869466.1:p.Gly375=
XM_017013978.2:c.1425C>A	XP_016869467.1:p.Gly475=
XM_017013979.2:c.522C>A	XP_016869468.1:p.Gly174=
XM_024447332.1:c.843C>A	XP_024303100.1:p.Gly281=
XM_024447333.1:c.441C>A	XP_024303101.1:p.Gly147=
NM_145201.6:c.1206C>A MANE Select	NP_660202.3:p.Gly402=
NM_001286829.2:c.1206C>A	NP_001273758.1:p.Gly402=