Canonical Allele Identifier: CA463375942

Gene: NAPRT

Linked Data

• MyVariant Identifiers: chr8:g.144657660C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143575490C>G , CM000670.2:g.143575490C>G	GRCh38
NC_000008.10:g.144657660C>G , CM000670.1:g.144657660C>G	GRCh37
NC_000008.9:g.144728803C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449291.7:c.1224G>C MANE Select	ENSP00000401508.2:p.Leu408=
ENST00000340490.7:c.1224G>C	ENSP00000341136.3:p.Leu408=
ENST00000426292.7:c.1224G>C	ENSP00000390949.3:p.Leu408=
ENST00000435154.7:c.1224G>C	ENSP00000405670.3:p.Leu408=
ENST00000449291.6:c.1224G>C	ENSP00000401508.2:p.Leu408=
ENST00000460623.5:c.202G>C
ENST00000464332.5:n.768G>C
ENST00000525583.5:c.1008G>C
NM_001286829.1:c.1224G>C	NP_001273758.1:p.Leu408=
NM_145201.5:c.1224G>C	NP_660202.3:p.Leu408=
XM_011517377.1:c.1224G>C	XP_011515679.1:p.Leu408=
NM_001363145.1:c.1143G>C	NP_001350074.1:p.Leu381=
NM_001363146.1:c.540G>C	NP_001350075.1:p.Leu180=
XM_017013975.2:c.1443G>C	XP_016869464.1:p.Leu481=
XM_017013976.2:c.1443G>C	XP_016869465.1:p.Leu481=
XM_017013977.2:c.1143G>C	XP_016869466.1:p.Leu381=
XM_017013978.2:c.1443G>C	XP_016869467.1:p.Leu481=
XM_017013979.2:c.540G>C	XP_016869468.1:p.Leu180=
XM_024447332.1:c.861G>C	XP_024303100.1:p.Leu287=
XM_024447333.1:c.459G>C	XP_024303101.1:p.Leu153=
NM_145201.6:c.1224G>C MANE Select	NP_660202.3:p.Leu408=
NM_001286829.2:c.1224G>C	NP_001273758.1:p.Leu408=