Canonical Allele Identifier: CA1742334878
Gene: IMPDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128401116C= , CM000669.2:g.128401116C= GRCh38
NC_000007.13:g.128041170C= , CM000669.1:g.128041170C= GRCh37
NC_000007.12:g.127828406C= NCBI36
NG_009194.1:g.13867G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000348127.11:c.295G= ENSP00000265385.8:p.Asp99=
ENST00000484496.6:n.259G=
ENST00000338791.11:c.403G= MANE Select ENSP00000345096.6:p.Asp135=
ENST00000648462.1:c.50G=
ENST00000338791.10:c.403G= ENSP00000345096.6:p.Asp135=
ENST00000348127.10:c.295G= ENSP00000265385.8:p.Asp99=
ENST00000354269.9:c.373G= ENSP00000346219.5:p.Asp125=
ENST00000419067.6:c.304G= ENSP00000399400.2:p.Asp102=
ENST00000469328.5:c.149G=
ENST00000470772.5:c.148G= ENSP00000417296.1:p.Asp50=
ENST00000473463.1:c.*149G= ENSP00000420469.1:n.*149G=
ENST00000480861.5:c.148G= ENSP00000420185.1:p.Asp50=
ENST00000484496.5:c.259G= ENSP00000418742.1:p.Asp87=
ENST00000489263.1:c.196G= ENSP00000418592.1:p.Asp66=
ENST00000491376.5:n.572G=
ENST00000496200.5:c.148G= ENSP00000420803.1:p.Asp50=
ENST00000496487.5:n.223G=
ENST00000497868.5:c.196G= ENSP00000419609.1:p.Asp66=
ENST00000626419.2:c.148G= ENSP00000486056.1:p.Asp50=
NM_000883.3:c.403G= NP_000874.2:p.Asp135=
NM_001102605.1:c.373G= NP_001096075.1:p.Asp125=
NM_001142573.1:c.148G= NP_001136045.1:p.Asp50=
NM_001142574.1:c.148G= NP_001136046.1:p.Asp50=
NM_001142575.1:c.148G= NP_001136047.1:p.Asp50=
NM_001142576.1:c.304G= NP_001136048.1:p.Asp102=
NM_001304521.1:c.196G= NP_001291450.1:p.Asp66=
NM_183243.2:c.295G= NP_899066.1:p.Asp99=
XM_005250314.1:c.172G= XP_005250371.1:p.Asp58=
XM_006715967.1:c.403G= XP_006716030.1:p.Asp135=
XM_006715968.1:c.373G= XP_006716031.1:p.Asp125=
XM_006715969.1:c.295G= XP_006716032.1:p.Asp99=
XM_006715970.2:c.196G= XP_006716033.1:p.Asp66=
XM_006715971.1:c.172G= XP_006716034.1:p.Asp58=
XM_017012172.1:c.172G= XP_016867661.1:p.Asp58=
XM_017012173.1:c.373G= XP_016867662.1:p.Asp125=
XM_024446755.1:c.373G= XP_024302523.1:p.Asp125=
XM_024446756.1:c.295G= XP_024302524.1:p.Asp99=
XM_024446757.1:c.196G= XP_024302525.1:p.Asp66=
XM_024446758.1:c.172G= XP_024302526.1:p.Asp58=
NM_000883.4:c.403G= MANE Select NP_000874.2:p.Asp135=
NM_001102605.2:c.373G= NP_001096075.1:p.Asp125=
NM_001142573.2:c.148G= NP_001136045.1:p.Asp50=
NM_001142574.2:c.148G= NP_001136046.1:p.Asp50=
NM_001142575.2:c.148G= NP_001136047.1:p.Asp50=
NM_001142576.2:c.304G= NP_001136048.1:p.Asp102=
NM_001304521.2:c.196G= NP_001291450.1:p.Asp66=
NM_183243.3:c.295G= NP_899066.1:p.Asp99=