Canonical Allele Identifier: CA369169226

Gene: IMPDH1

Linked Data

• ClinVar Variation Id: 866754
• ClinVar RCV Id: RCV001075040
• dbSNP Id: rs1798089372
• gnomAD v4: 7-128398541-C-T
• MyVariant Identifiers: chr7:g.128038595C>T (hg19) ; chr7:g.128398541C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128398541C>T , CM000669.2:g.128398541C>T	GRCh38
NC_000007.13:g.128038595C>T , CM000669.1:g.128038595C>T	GRCh37
NC_000007.12:g.127825831C>T	NCBI36
NG_009194.1:g.16442G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348127.11:c.839G>A	ENSP00000265385.8:p.Arg280Gln
ENST00000484496.6:n.822G>A
ENST00000338791.11:c.947G>A MANE Select	ENSP00000345096.6:p.Arg316Gln
ENST00000648462.1:c.579G>A
ENST00000338791.10:c.947G>A	ENSP00000345096.6:p.Arg316Gln
ENST00000348127.10:c.839G>A	ENSP00000265385.8:p.Arg280Gln
ENST00000354269.9:c.917G>A	ENSP00000346219.5:p.Arg306Gln
ENST00000419067.6:c.848G>A	ENSP00000399400.2:p.Arg283Gln
ENST00000468842.1:n.536G>A
ENST00000469328.5:c.712G>A
ENST00000470772.5:c.689G>A	ENSP00000417296.1:p.Arg230Gln
ENST00000480861.5:c.677G>A	ENSP00000420185.1:p.Arg226Gln
ENST00000484496.5:c.822G>A	ENSP00000418742.1:n.822G>A
ENST00000496200.5:c.617G>A	ENSP00000420803.1:p.Arg206Gln
ENST00000497868.5:c.740G>A	ENSP00000419609.1:p.Arg247Gln
ENST00000626419.2:c.689G>A	ENSP00000486056.1:p.Arg230Gln
NM_000883.3:c.947G>A	NP_000874.2:p.Arg316Gln
NM_001102605.1:c.917G>A	NP_001096075.1:p.Arg306Gln
NM_001142573.1:c.692G>A	NP_001136045.1:p.Arg231Gln
NM_001142574.1:c.677G>A	NP_001136046.1:p.Arg226Gln
NM_001142575.1:c.617G>A	NP_001136047.1:p.Arg206Gln
NM_001142576.1:c.848G>A	NP_001136048.1:p.Arg283Gln
NM_001304521.1:c.740G>A	NP_001291450.1:p.Arg247Gln
NM_183243.2:c.839G>A	NP_899066.1:p.Arg280Gln
XM_005250314.1:c.716G>A	XP_005250371.1:p.Arg239Gln
XM_006715967.1:c.947G>A	XP_006716030.1:p.Arg316Gln
XM_006715968.1:c.917G>A	XP_006716031.1:p.Arg306Gln
XM_006715969.1:c.839G>A	XP_006716032.1:p.Arg280Gln
XM_006715970.2:c.740G>A	XP_006716033.1:p.Arg247Gln
XM_006715971.1:c.716G>A	XP_006716034.1:p.Arg239Gln
XM_011516156.1:c.329G>A	XP_011514458.1:p.Arg110Gln
XM_011516157.1:c.329G>A	XP_011514459.1:p.Arg110Gln
XM_017012172.1:c.716G>A	XP_016867661.1:p.Arg239Gln
XM_017012173.1:c.917G>A	XP_016867662.1:p.Arg306Gln
XM_024446755.1:c.917G>A	XP_024302523.1:p.Arg306Gln
XM_024446756.1:c.839G>A	XP_024302524.1:p.Arg280Gln
XM_024446757.1:c.740G>A	XP_024302525.1:p.Arg247Gln
XM_024446758.1:c.716G>A	XP_024302526.1:p.Arg239Gln
NM_000883.4:c.947G>A MANE Select	NP_000874.2:p.Arg316Gln
NM_001102605.2:c.917G>A	NP_001096075.1:p.Arg306Gln
NM_001142573.2:c.692G>A	NP_001136045.1:p.Arg231Gln
NM_001142574.2:c.677G>A	NP_001136046.1:p.Arg226Gln
NM_001142575.2:c.617G>A	NP_001136047.1:p.Arg206Gln
NM_001142576.2:c.848G>A	NP_001136048.1:p.Arg283Gln
NM_001304521.2:c.740G>A	NP_001291450.1:p.Arg247Gln
NM_183243.3:c.839G>A	NP_899066.1:p.Arg280Gln