Canonical Allele Identifier: CA369169497

Gene: IMPDH1

Linked Data

• dbSNP Id: rs1490614147
• gnomAD v2: 7-128038623-T-C
• gnomAD v4: 7-128398569-T-C
• MyVariant Identifiers: chr7:g.128038623T>C (hg19) ; chr7:g.128398569T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128398569T>C , CM000669.2:g.128398569T>C	GRCh38
NC_000007.13:g.128038623T>C , CM000669.1:g.128038623T>C	GRCh37
NC_000007.12:g.127825859T>C	NCBI36
NG_009194.1:g.16414A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000348127.11:c.811A>G	ENSP00000265385.8:p.Ile271Val
ENST00000484496.6:n.794A>G
ENST00000338791.11:c.919A>G MANE Select	ENSP00000345096.6:p.Ile307Val
ENST00000648462.1:c.551A>G
ENST00000338791.10:c.919A>G	ENSP00000345096.6:p.Ile307Val
ENST00000348127.10:c.811A>G	ENSP00000265385.8:p.Ile271Val
ENST00000354269.9:c.889A>G	ENSP00000346219.5:p.Ile297Val
ENST00000419067.6:c.820A>G	ENSP00000399400.2:p.Ile274Val
ENST00000468842.1:n.508A>G
ENST00000469328.5:c.684A>G
ENST00000470772.5:c.661A>G	ENSP00000417296.1:p.Ile221Val
ENST00000480861.5:c.649A>G	ENSP00000420185.1:p.Ile217Val
ENST00000484496.5:c.794A>G	ENSP00000418742.1:n.794A>G
ENST00000496200.5:c.589A>G	ENSP00000420803.1:p.Ile197Val
ENST00000497868.5:c.712A>G	ENSP00000419609.1:p.Ile238Val
ENST00000626419.2:c.661A>G	ENSP00000486056.1:p.Ile221Val
NM_000883.3:c.919A>G	NP_000874.2:p.Ile307Val
NM_001102605.1:c.889A>G	NP_001096075.1:p.Ile297Val
NM_001142573.1:c.664A>G	NP_001136045.1:p.Ile222Val
NM_001142574.1:c.649A>G	NP_001136046.1:p.Ile217Val
NM_001142575.1:c.589A>G	NP_001136047.1:p.Ile197Val
NM_001142576.1:c.820A>G	NP_001136048.1:p.Ile274Val
NM_001304521.1:c.712A>G	NP_001291450.1:p.Ile238Val
NM_183243.2:c.811A>G	NP_899066.1:p.Ile271Val
XM_005250314.1:c.688A>G	XP_005250371.1:p.Ile230Val
XM_006715967.1:c.919A>G	XP_006716030.1:p.Ile307Val
XM_006715968.1:c.889A>G	XP_006716031.1:p.Ile297Val
XM_006715969.1:c.811A>G	XP_006716032.1:p.Ile271Val
XM_006715970.2:c.712A>G	XP_006716033.1:p.Ile238Val
XM_006715971.1:c.688A>G	XP_006716034.1:p.Ile230Val
XM_011516156.1:c.301A>G	XP_011514458.1:p.Ile101Val
XM_011516157.1:c.301A>G	XP_011514459.1:p.Ile101Val
XM_017012172.1:c.688A>G	XP_016867661.1:p.Ile230Val
XM_017012173.1:c.889A>G	XP_016867662.1:p.Ile297Val
XM_024446755.1:c.889A>G	XP_024302523.1:p.Ile297Val
XM_024446756.1:c.811A>G	XP_024302524.1:p.Ile271Val
XM_024446757.1:c.712A>G	XP_024302525.1:p.Ile238Val
XM_024446758.1:c.688A>G	XP_024302526.1:p.Ile230Val
NM_000883.4:c.919A>G MANE Select	NP_000874.2:p.Ile307Val
NM_001102605.2:c.889A>G	NP_001096075.1:p.Ile297Val
NM_001142573.2:c.664A>G	NP_001136045.1:p.Ile222Val
NM_001142574.2:c.649A>G	NP_001136046.1:p.Ile217Val
NM_001142575.2:c.589A>G	NP_001136047.1:p.Ile197Val
NM_001142576.2:c.820A>G	NP_001136048.1:p.Ile274Val
NM_001304521.2:c.712A>G	NP_001291450.1:p.Ile238Val
NM_183243.3:c.811A>G	NP_899066.1:p.Ile271Val