Canonical Allele Identifier: CA457528180

Gene: IMPDH1

Linked Data

• MyVariant Identifiers: chr7:g.128038495G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128398441G>C , CM000669.2:g.128398441G>C	GRCh38
NC_000007.13:g.128038495G>C , CM000669.1:g.128038495G>C	GRCh37
NC_000007.12:g.127825731G>C	NCBI36
NG_009194.1:g.16542C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348127.11:c.939C>G	ENSP00000265385.8:p.Thr313=
ENST00000484496.6:n.922C>G
ENST00000338791.11:c.1047C>G MANE Select	ENSP00000345096.6:p.Thr349=
ENST00000648462.1:c.679C>G
ENST00000338791.10:c.1047C>G	ENSP00000345096.6:p.Thr349=
ENST00000348127.10:c.939C>G	ENSP00000265385.8:p.Thr313=
ENST00000354269.9:c.1017C>G	ENSP00000346219.5:p.Thr339=
ENST00000419067.6:c.948C>G	ENSP00000399400.2:p.Thr316=
ENST00000469328.5:c.812C>G
ENST00000470772.5:c.789C>G	ENSP00000417296.1:p.Thr263=
ENST00000480861.5:c.777C>G	ENSP00000420185.1:p.Thr259=
ENST00000484496.5:c.922C>G	ENSP00000418742.1:n.922C>G
ENST00000496200.5:c.717C>G	ENSP00000420803.1:p.Thr239=
ENST00000497868.5:c.840C>G	ENSP00000419609.1:p.Thr280=
ENST00000626419.2:c.789C>G	ENSP00000486056.1:p.Thr263=
NM_000883.3:c.1047C>G	NP_000874.2:p.Thr349=
NM_001102605.1:c.1017C>G	NP_001096075.1:p.Thr339=
NM_001142573.1:c.792C>G	NP_001136045.1:p.Thr264=
NM_001142574.1:c.777C>G	NP_001136046.1:p.Thr259=
NM_001142575.1:c.717C>G	NP_001136047.1:p.Thr239=
NM_001142576.1:c.948C>G	NP_001136048.1:p.Thr316=
NM_001304521.1:c.840C>G	NP_001291450.1:p.Thr280=
NM_183243.2:c.939C>G	NP_899066.1:p.Thr313=
XM_005250314.1:c.816C>G	XP_005250371.1:p.Thr272=
XM_006715967.1:c.1047C>G	XP_006716030.1:p.Thr349=
XM_006715968.1:c.1017C>G	XP_006716031.1:p.Thr339=
XM_006715969.1:c.939C>G	XP_006716032.1:p.Thr313=
XM_006715970.2:c.840C>G	XP_006716033.1:p.Thr280=
XM_006715971.1:c.816C>G	XP_006716034.1:p.Thr272=
XM_011516156.1:c.429C>G	XP_011514458.1:p.Thr143=
XM_011516157.1:c.429C>G	XP_011514459.1:p.Thr143=
XM_017012172.1:c.816C>G	XP_016867661.1:p.Thr272=
XM_017012173.1:c.1017C>G	XP_016867662.1:p.Thr339=
XM_024446755.1:c.1017C>G	XP_024302523.1:p.Thr339=
XM_024446756.1:c.939C>G	XP_024302524.1:p.Thr313=
XM_024446757.1:c.840C>G	XP_024302525.1:p.Thr280=
XM_024446758.1:c.816C>G	XP_024302526.1:p.Thr272=
NM_000883.4:c.1047C>G MANE Select	NP_000874.2:p.Thr349=
NM_001102605.2:c.1017C>G	NP_001096075.1:p.Thr339=
NM_001142573.2:c.792C>G	NP_001136045.1:p.Thr264=
NM_001142574.2:c.777C>G	NP_001136046.1:p.Thr259=
NM_001142575.2:c.717C>G	NP_001136047.1:p.Thr239=
NM_001142576.2:c.948C>G	NP_001136048.1:p.Thr316=
NM_001304521.2:c.840C>G	NP_001291450.1:p.Thr280=
NM_183243.3:c.939C>G	NP_899066.1:p.Thr313=