Canonical Allele Identifier: CA369174556

Gene: IMPDH1

Linked Data

• MyVariant Identifiers: chr7:g.128041139G>C (hg19) ; chr7:g.128401085G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128401085G>C , CM000669.2:g.128401085G>C	GRCh38
NC_000007.13:g.128041139G>C , CM000669.1:g.128041139G>C	GRCh37
NC_000007.12:g.127828375G>C	NCBI36
NG_009194.1:g.13898C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348127.11:c.326C>G	ENSP00000265385.8:p.Thr109Arg
ENST00000484496.6:n.290C>G
ENST00000338791.11:c.434C>G MANE Select	ENSP00000345096.6:p.Thr145Arg
ENST00000648462.1:c.81C>G
ENST00000338791.10:c.434C>G	ENSP00000345096.6:p.Thr145Arg
ENST00000348127.10:c.326C>G	ENSP00000265385.8:p.Thr109Arg
ENST00000354269.9:c.404C>G	ENSP00000346219.5:p.Thr135Arg
ENST00000419067.6:c.335C>G	ENSP00000399400.2:p.Thr112Arg
ENST00000469328.5:c.180C>G
ENST00000470772.5:c.179C>G	ENSP00000417296.1:p.Thr60Arg
ENST00000473463.1:c.*180C>G	ENSP00000420469.1:n.*180C>G
ENST00000480861.5:c.179C>G	ENSP00000420185.1:p.Thr60Arg
ENST00000484496.5:c.290C>G	ENSP00000418742.1:p.Thr97Arg
ENST00000489263.1:c.227C>G	ENSP00000418592.1:p.Thr76Arg
ENST00000491376.5:n.603C>G
ENST00000496200.5:c.179C>G	ENSP00000420803.1:p.Thr60Arg
ENST00000496487.5:n.254C>G
ENST00000497868.5:c.227C>G	ENSP00000419609.1:p.Thr76Arg
ENST00000626419.2:c.179C>G	ENSP00000486056.1:p.Thr60Arg
NM_000883.3:c.434C>G	NP_000874.2:p.Thr145Arg
NM_001102605.1:c.404C>G	NP_001096075.1:p.Thr135Arg
NM_001142573.1:c.179C>G	NP_001136045.1:p.Thr60Arg
NM_001142574.1:c.179C>G	NP_001136046.1:p.Thr60Arg
NM_001142575.1:c.179C>G	NP_001136047.1:p.Thr60Arg
NM_001142576.1:c.335C>G	NP_001136048.1:p.Thr112Arg
NM_001304521.1:c.227C>G	NP_001291450.1:p.Thr76Arg
NM_183243.2:c.326C>G	NP_899066.1:p.Thr109Arg
XM_005250314.1:c.203C>G	XP_005250371.1:p.Thr68Arg
XM_006715967.1:c.434C>G	XP_006716030.1:p.Thr145Arg
XM_006715968.1:c.404C>G	XP_006716031.1:p.Thr135Arg
XM_006715969.1:c.326C>G	XP_006716032.1:p.Thr109Arg
XM_006715970.2:c.227C>G	XP_006716033.1:p.Thr76Arg
XM_006715971.1:c.203C>G	XP_006716034.1:p.Thr68Arg
XM_017012172.1:c.203C>G	XP_016867661.1:p.Thr68Arg
XM_017012173.1:c.404C>G	XP_016867662.1:p.Thr135Arg
XM_024446755.1:c.404C>G	XP_024302523.1:p.Thr135Arg
XM_024446756.1:c.326C>G	XP_024302524.1:p.Thr109Arg
XM_024446757.1:c.227C>G	XP_024302525.1:p.Thr76Arg
XM_024446758.1:c.203C>G	XP_024302526.1:p.Thr68Arg
NM_000883.4:c.434C>G MANE Select	NP_000874.2:p.Thr145Arg
NM_001102605.2:c.404C>G	NP_001096075.1:p.Thr135Arg
NM_001142573.2:c.179C>G	NP_001136045.1:p.Thr60Arg
NM_001142574.2:c.179C>G	NP_001136046.1:p.Thr60Arg
NM_001142575.2:c.179C>G	NP_001136047.1:p.Thr60Arg
NM_001142576.2:c.335C>G	NP_001136048.1:p.Thr112Arg
NM_001304521.2:c.227C>G	NP_001291450.1:p.Thr76Arg
NM_183243.3:c.326C>G	NP_899066.1:p.Thr109Arg