Canonical Allele Identifier: CA369169344
Gene: IMPDH1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128398550T>A , CM000669.2:g.128398550T>A GRCh38
NC_000007.13:g.128038604T>A , CM000669.1:g.128038604T>A GRCh37
NC_000007.12:g.127825840T>A NCBI36
NG_009194.1:g.16433A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000348127.11:c.830A>T ENSP00000265385.8:p.Lys277Met
ENST00000484496.6:n.813A>T
ENST00000338791.11:c.938A>T MANE Select ENSP00000345096.6:p.Lys313Met
ENST00000648462.1:c.570A>T
ENST00000338791.10:c.938A>T ENSP00000345096.6:p.Lys313Met
ENST00000348127.10:c.830A>T ENSP00000265385.8:p.Lys277Met
ENST00000354269.9:c.908A>T ENSP00000346219.5:p.Lys303Met
ENST00000419067.6:c.839A>T ENSP00000399400.2:p.Lys280Met
ENST00000468842.1:n.527A>T
ENST00000469328.5:c.703A>T
ENST00000470772.5:c.680A>T ENSP00000417296.1:p.Lys227Met
ENST00000480861.5:c.668A>T ENSP00000420185.1:p.Lys223Met
ENST00000484496.5:c.813A>T ENSP00000418742.1:n.813A>T
ENST00000496200.5:c.608A>T ENSP00000420803.1:p.Lys203Met
ENST00000497868.5:c.731A>T ENSP00000419609.1:p.Lys244Met
ENST00000626419.2:c.680A>T ENSP00000486056.1:p.Lys227Met
NM_000883.3:c.938A>T NP_000874.2:p.Lys313Met
NM_001102605.1:c.908A>T NP_001096075.1:p.Lys303Met
NM_001142573.1:c.683A>T NP_001136045.1:p.Lys228Met
NM_001142574.1:c.668A>T NP_001136046.1:p.Lys223Met
NM_001142575.1:c.608A>T NP_001136047.1:p.Lys203Met
NM_001142576.1:c.839A>T NP_001136048.1:p.Lys280Met
NM_001304521.1:c.731A>T NP_001291450.1:p.Lys244Met
NM_183243.2:c.830A>T NP_899066.1:p.Lys277Met
XM_005250314.1:c.707A>T XP_005250371.1:p.Lys236Met
XM_006715967.1:c.938A>T XP_006716030.1:p.Lys313Met
XM_006715968.1:c.908A>T XP_006716031.1:p.Lys303Met
XM_006715969.1:c.830A>T XP_006716032.1:p.Lys277Met
XM_006715970.2:c.731A>T XP_006716033.1:p.Lys244Met
XM_006715971.1:c.707A>T XP_006716034.1:p.Lys236Met
XM_011516156.1:c.320A>T XP_011514458.1:p.Lys107Met
XM_011516157.1:c.320A>T XP_011514459.1:p.Lys107Met
XM_017012172.1:c.707A>T XP_016867661.1:p.Lys236Met
XM_017012173.1:c.908A>T XP_016867662.1:p.Lys303Met
XM_024446755.1:c.908A>T XP_024302523.1:p.Lys303Met
XM_024446756.1:c.830A>T XP_024302524.1:p.Lys277Met
XM_024446757.1:c.731A>T XP_024302525.1:p.Lys244Met
XM_024446758.1:c.707A>T XP_024302526.1:p.Lys236Met
NM_000883.4:c.938A>T MANE Select NP_000874.2:p.Lys313Met
NM_001102605.2:c.908A>T NP_001096075.1:p.Lys303Met
NM_001142573.2:c.683A>T NP_001136045.1:p.Lys228Met
NM_001142574.2:c.668A>T NP_001136046.1:p.Lys223Met
NM_001142575.2:c.608A>T NP_001136047.1:p.Lys203Met
NM_001142576.2:c.839A>T NP_001136048.1:p.Lys280Met
NM_001304521.2:c.731A>T NP_001291450.1:p.Lys244Met
NM_183243.3:c.830A>T NP_899066.1:p.Lys277Met