Canonical Allele Identifier: CA369169473

Gene: IMPDH1

Linked Data

• ClinVar Variation Id: 860766
• ClinVar RCV Id: RCV001067136
• dbSNP Id: rs1798092833
• gnomAD v4: 7-128398566-C-T
• MyVariant Identifiers: chr7:g.128038620C>T (hg19) ; chr7:g.128398566C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128398566C>T , CM000669.2:g.128398566C>T	GRCh38
NC_000007.13:g.128038620C>T , CM000669.1:g.128038620C>T	GRCh37
NC_000007.12:g.127825856C>T	NCBI36
NG_009194.1:g.16417G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000348127.11:c.814G>A	ENSP00000265385.8:p.Ala272Thr
ENST00000484496.6:n.797G>A
ENST00000338791.11:c.922G>A MANE Select	ENSP00000345096.6:p.Ala308Thr
ENST00000648462.1:c.554G>A
ENST00000338791.10:c.922G>A	ENSP00000345096.6:p.Ala308Thr
ENST00000348127.10:c.814G>A	ENSP00000265385.8:p.Ala272Thr
ENST00000354269.9:c.892G>A	ENSP00000346219.5:p.Ala298Thr
ENST00000419067.6:c.823G>A	ENSP00000399400.2:p.Ala275Thr
ENST00000468842.1:n.511G>A
ENST00000469328.5:c.687G>A
ENST00000470772.5:c.664G>A	ENSP00000417296.1:p.Ala222Thr
ENST00000480861.5:c.652G>A	ENSP00000420185.1:p.Ala218Thr
ENST00000484496.5:c.797G>A	ENSP00000418742.1:n.797G>A
ENST00000496200.5:c.592G>A	ENSP00000420803.1:p.Ala198Thr
ENST00000497868.5:c.715G>A	ENSP00000419609.1:p.Ala239Thr
ENST00000626419.2:c.664G>A	ENSP00000486056.1:p.Ala222Thr
NM_000883.3:c.922G>A	NP_000874.2:p.Ala308Thr
NM_001102605.1:c.892G>A	NP_001096075.1:p.Ala298Thr
NM_001142573.1:c.667G>A	NP_001136045.1:p.Ala223Thr
NM_001142574.1:c.652G>A	NP_001136046.1:p.Ala218Thr
NM_001142575.1:c.592G>A	NP_001136047.1:p.Ala198Thr
NM_001142576.1:c.823G>A	NP_001136048.1:p.Ala275Thr
NM_001304521.1:c.715G>A	NP_001291450.1:p.Ala239Thr
NM_183243.2:c.814G>A	NP_899066.1:p.Ala272Thr
XM_005250314.1:c.691G>A	XP_005250371.1:p.Ala231Thr
XM_006715967.1:c.922G>A	XP_006716030.1:p.Ala308Thr
XM_006715968.1:c.892G>A	XP_006716031.1:p.Ala298Thr
XM_006715969.1:c.814G>A	XP_006716032.1:p.Ala272Thr
XM_006715970.2:c.715G>A	XP_006716033.1:p.Ala239Thr
XM_006715971.1:c.691G>A	XP_006716034.1:p.Ala231Thr
XM_011516156.1:c.304G>A	XP_011514458.1:p.Ala102Thr
XM_011516157.1:c.304G>A	XP_011514459.1:p.Ala102Thr
XM_017012172.1:c.691G>A	XP_016867661.1:p.Ala231Thr
XM_017012173.1:c.892G>A	XP_016867662.1:p.Ala298Thr
XM_024446755.1:c.892G>A	XP_024302523.1:p.Ala298Thr
XM_024446756.1:c.814G>A	XP_024302524.1:p.Ala272Thr
XM_024446757.1:c.715G>A	XP_024302525.1:p.Ala239Thr
XM_024446758.1:c.691G>A	XP_024302526.1:p.Ala231Thr
NM_000883.4:c.922G>A MANE Select	NP_000874.2:p.Ala308Thr
NM_001102605.2:c.892G>A	NP_001096075.1:p.Ala298Thr
NM_001142573.2:c.667G>A	NP_001136045.1:p.Ala223Thr
NM_001142574.2:c.652G>A	NP_001136046.1:p.Ala218Thr
NM_001142575.2:c.592G>A	NP_001136047.1:p.Ala198Thr
NM_001142576.2:c.823G>A	NP_001136048.1:p.Ala275Thr
NM_001304521.2:c.715G>A	NP_001291450.1:p.Ala239Thr
NM_183243.3:c.814G>A	NP_899066.1:p.Ala272Thr