Canonical Allele Identifier: CA1742366509
Gene: IMPDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128398442G= , CM000669.2:g.128398442G= GRCh38
NC_000007.13:g.128038496G= , CM000669.1:g.128038496G= GRCh37
NC_000007.12:g.127825732G= NCBI36
NG_009194.1:g.16541C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000348127.11:c.938C= ENSP00000265385.8:p.Thr313=
ENST00000484496.6:n.921C=
ENST00000338791.11:c.1046C= MANE Select ENSP00000345096.6:p.Thr349=
ENST00000648462.1:c.678C=
ENST00000338791.10:c.1046C= ENSP00000345096.6:p.Thr349=
ENST00000348127.10:c.938C= ENSP00000265385.8:p.Thr313=
ENST00000354269.9:c.1016C= ENSP00000346219.5:p.Thr339=
ENST00000419067.6:c.947C= ENSP00000399400.2:p.Thr316=
ENST00000469328.5:c.811C=
ENST00000470772.5:c.788C= ENSP00000417296.1:p.Thr263=
ENST00000480861.5:c.776C= ENSP00000420185.1:p.Thr259=
ENST00000484496.5:c.921C= ENSP00000418742.1:n.921C=
ENST00000496200.5:c.716C= ENSP00000420803.1:p.Thr239=
ENST00000497868.5:c.839C= ENSP00000419609.1:p.Thr280=
ENST00000626419.2:c.788C= ENSP00000486056.1:p.Thr263=
NM_000883.3:c.1046C= NP_000874.2:p.Thr349=
NM_001102605.1:c.1016C= NP_001096075.1:p.Thr339=
NM_001142573.1:c.791C= NP_001136045.1:p.Thr264=
NM_001142574.1:c.776C= NP_001136046.1:p.Thr259=
NM_001142575.1:c.716C= NP_001136047.1:p.Thr239=
NM_001142576.1:c.947C= NP_001136048.1:p.Thr316=
NM_001304521.1:c.839C= NP_001291450.1:p.Thr280=
NM_183243.2:c.938C= NP_899066.1:p.Thr313=
XM_005250314.1:c.815C= XP_005250371.1:p.Thr272=
XM_006715967.1:c.1046C= XP_006716030.1:p.Thr349=
XM_006715968.1:c.1016C= XP_006716031.1:p.Thr339=
XM_006715969.1:c.938C= XP_006716032.1:p.Thr313=
XM_006715970.2:c.839C= XP_006716033.1:p.Thr280=
XM_006715971.1:c.815C= XP_006716034.1:p.Thr272=
XM_011516156.1:c.428C= XP_011514458.1:p.Thr143=
XM_011516157.1:c.428C= XP_011514459.1:p.Thr143=
XM_017012172.1:c.815C= XP_016867661.1:p.Thr272=
XM_017012173.1:c.1016C= XP_016867662.1:p.Thr339=
XM_024446755.1:c.1016C= XP_024302523.1:p.Thr339=
XM_024446756.1:c.938C= XP_024302524.1:p.Thr313=
XM_024446757.1:c.839C= XP_024302525.1:p.Thr280=
XM_024446758.1:c.815C= XP_024302526.1:p.Thr272=
NM_000883.4:c.1046C= MANE Select NP_000874.2:p.Thr349=
NM_001102605.2:c.1016C= NP_001096075.1:p.Thr339=
NM_001142573.2:c.791C= NP_001136045.1:p.Thr264=
NM_001142574.2:c.776C= NP_001136046.1:p.Thr259=
NM_001142575.2:c.716C= NP_001136047.1:p.Thr239=
NM_001142576.2:c.947C= NP_001136048.1:p.Thr316=
NM_001304521.2:c.839C= NP_001291450.1:p.Thr280=
NM_183243.3:c.938C= NP_899066.1:p.Thr313=