Canonical Allele Identifier: CA1742334633

Gene: IMPDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128400982_128400983delinsGC , CM000669.2:g.128400982_128400983delinsGC	GRCh38
NC_000007.13:g.128041036_128041037delinsGC , CM000669.1:g.128041036_128041037delinsGC	GRCh37
NC_000007.12:g.127828272_127828273delinsGC	NCBI36
NG_009194.1:g.14000_14001delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348127.11:c.396+32_396+33delinsGC	ENSP00000265385.8:n.396+32_396+33delinsGC
ENST00000484496.6:n.360+32_360+33delinsGC
ENST00000338791.11:c.504+32_504+33delinsGC MANE Select	ENSP00000345096.6:n.504+32_504+33delinsGC
ENST00000648462.1:c.151+32_151+33delinsGC
ENST00000338791.10:c.504+32_504+33delinsGC	ENSP00000345096.6:n.504+32_504+33delinsGC
ENST00000348127.10:c.396+32_396+33delinsGC	ENSP00000265385.8:n.396+32_396+33delinsGC
ENST00000354269.9:c.474+32_474+33delinsGC	ENSP00000346219.5:n.474+32_474+33delinsGC
ENST00000419067.6:c.405+32_405+33delinsGC	ENSP00000399400.2:n.405+32_405+33delinsGC
ENST00000469328.5:c.250+32_250+33delinsGC
ENST00000470772.5:c.249+32_249+33delinsGC	ENSP00000417296.1:n.249+32_249+33delinsGC
ENST00000473463.1:c.*250+32_*250+33delinsGC	ENSP00000420469.1:n.*250+32_*250+33delinsGC
ENST00000480861.5:c.249+32_249+33delinsGC	ENSP00000420185.1:n.249+32_249+33delinsGC
ENST00000484496.5:c.360+32_360+33delinsGC	ENSP00000418742.1:n.360+32_360+33delinsGC
ENST00000489263.1:c.297+32_297+33delinsGC	ENSP00000418592.1:n.297+32_297+33delinsGC
ENST00000491376.5:n.673+32_673+33delinsGC
ENST00000496200.5:c.249+32_249+33delinsGC	ENSP00000420803.1:n.249+32_249+33delinsGC
ENST00000496487.5:n.324+32_324+33delinsGC
ENST00000497868.5:c.297+32_297+33delinsGC	ENSP00000419609.1:n.297+32_297+33delinsGC
ENST00000626419.2:c.249+32_249+33delinsGC	ENSP00000486056.1:n.249+32_249+33delinsGC
NM_000883.3:c.504+32_504+33delinsGC	NP_000874.2:n.504+32_504+33delinsGC
NM_001102605.1:c.474+32_474+33delinsGC	NP_001096075.1:n.474+32_474+33delinsGC
NM_001142573.1:c.249+32_249+33delinsGC	NP_001136045.1:n.249+32_249+33delinsGC
NM_001142574.1:c.249+32_249+33delinsGC	NP_001136046.1:n.249+32_249+33delinsGC
NM_001142575.1:c.249+32_249+33delinsGC	NP_001136047.1:n.249+32_249+33delinsGC
NM_001142576.1:c.405+32_405+33delinsGC	NP_001136048.1:n.405+32_405+33delinsGC
NM_001304521.1:c.297+32_297+33delinsGC	NP_001291450.1:n.297+32_297+33delinsGC
NM_183243.2:c.396+32_396+33delinsGC	NP_899066.1:n.396+32_396+33delinsGC
XM_005250314.1:c.273+32_273+33delinsGC	XP_005250371.1:n.273+32_273+33delinsGC
XM_006715967.1:c.504+32_504+33delinsGC	XP_006716030.1:n.504+32_504+33delinsGC
XM_006715968.1:c.474+32_474+33delinsGC	XP_006716031.1:n.474+32_474+33delinsGC
XM_006715969.1:c.396+32_396+33delinsGC	XP_006716032.1:n.396+32_396+33delinsGC
XM_006715970.2:c.297+32_297+33delinsGC	XP_006716033.1:n.297+32_297+33delinsGC
XM_006715971.1:c.273+32_273+33delinsGC	XP_006716034.1:n.273+32_273+33delinsGC
XM_017012172.1:c.273+32_273+33delinsGC	XP_016867661.1:n.273+32_273+33delinsGC
XM_017012173.1:c.474+32_474+33delinsGC	XP_016867662.1:n.474+32_474+33delinsGC
XM_024446755.1:c.474+32_474+33delinsGC	XP_024302523.1:n.474+32_474+33delinsGC
XM_024446756.1:c.396+32_396+33delinsGC	XP_024302524.1:n.396+32_396+33delinsGC
XM_024446757.1:c.297+32_297+33delinsGC	XP_024302525.1:n.297+32_297+33delinsGC
XM_024446758.1:c.273+32_273+33delinsGC	XP_024302526.1:n.273+32_273+33delinsGC
NM_000883.4:c.504+32_504+33delinsGC MANE Select	NP_000874.2:n.504+32_504+33delinsGC
NM_001102605.2:c.474+32_474+33delinsGC	NP_001096075.1:n.474+32_474+33delinsGC
NM_001142573.2:c.249+32_249+33delinsGC	NP_001136045.1:n.249+32_249+33delinsGC
NM_001142574.2:c.249+32_249+33delinsGC	NP_001136046.1:n.249+32_249+33delinsGC
NM_001142575.2:c.249+32_249+33delinsGC	NP_001136047.1:n.249+32_249+33delinsGC
NM_001142576.2:c.405+32_405+33delinsGC	NP_001136048.1:n.405+32_405+33delinsGC
NM_001304521.2:c.297+32_297+33delinsGC	NP_001291450.1:n.297+32_297+33delinsGC
NM_183243.3:c.396+32_396+33delinsGC	NP_899066.1:n.396+32_396+33delinsGC