Canonical Allele Identifier: CA369168661

Gene: IMPDH1

Linked Data

• MyVariant Identifiers: chr7:g.128038548C>G (hg19) ; chr7:g.128398494C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128398494C>G , CM000669.2:g.128398494C>G	GRCh38
NC_000007.13:g.128038548C>G , CM000669.1:g.128038548C>G	GRCh37
NC_000007.12:g.127825784C>G	NCBI36
NG_009194.1:g.16489G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348127.11:c.886G>C	ENSP00000265385.8:p.Gly296Arg
ENST00000484496.6:n.869G>C
ENST00000338791.11:c.994G>C MANE Select	ENSP00000345096.6:p.Gly332Arg
ENST00000648462.1:c.626G>C
ENST00000338791.10:c.994G>C	ENSP00000345096.6:p.Gly332Arg
ENST00000348127.10:c.886G>C	ENSP00000265385.8:p.Gly296Arg
ENST00000354269.9:c.964G>C	ENSP00000346219.5:p.Gly322Arg
ENST00000419067.6:c.895G>C	ENSP00000399400.2:p.Gly299Arg
ENST00000468842.1:n.583G>C
ENST00000469328.5:c.759G>C
ENST00000470772.5:c.736G>C	ENSP00000417296.1:p.Gly246Arg
ENST00000480861.5:c.724G>C	ENSP00000420185.1:p.Gly242Arg
ENST00000484496.5:c.869G>C	ENSP00000418742.1:n.869G>C
ENST00000496200.5:c.664G>C	ENSP00000420803.1:p.Gly222Arg
ENST00000497868.5:c.787G>C	ENSP00000419609.1:p.Gly263Arg
ENST00000626419.2:c.736G>C	ENSP00000486056.1:p.Gly246Arg
NM_000883.3:c.994G>C	NP_000874.2:p.Gly332Arg
NM_001102605.1:c.964G>C	NP_001096075.1:p.Gly322Arg
NM_001142573.1:c.739G>C	NP_001136045.1:p.Gly247Arg
NM_001142574.1:c.724G>C	NP_001136046.1:p.Gly242Arg
NM_001142575.1:c.664G>C	NP_001136047.1:p.Gly222Arg
NM_001142576.1:c.895G>C	NP_001136048.1:p.Gly299Arg
NM_001304521.1:c.787G>C	NP_001291450.1:p.Gly263Arg
NM_183243.2:c.886G>C	NP_899066.1:p.Gly296Arg
XM_005250314.1:c.763G>C	XP_005250371.1:p.Gly255Arg
XM_006715967.1:c.994G>C	XP_006716030.1:p.Gly332Arg
XM_006715968.1:c.964G>C	XP_006716031.1:p.Gly322Arg
XM_006715969.1:c.886G>C	XP_006716032.1:p.Gly296Arg
XM_006715970.2:c.787G>C	XP_006716033.1:p.Gly263Arg
XM_006715971.1:c.763G>C	XP_006716034.1:p.Gly255Arg
XM_011516156.1:c.376G>C	XP_011514458.1:p.Gly126Arg
XM_011516157.1:c.376G>C	XP_011514459.1:p.Gly126Arg
XM_017012172.1:c.763G>C	XP_016867661.1:p.Gly255Arg
XM_017012173.1:c.964G>C	XP_016867662.1:p.Gly322Arg
XM_024446755.1:c.964G>C	XP_024302523.1:p.Gly322Arg
XM_024446756.1:c.886G>C	XP_024302524.1:p.Gly296Arg
XM_024446757.1:c.787G>C	XP_024302525.1:p.Gly263Arg
XM_024446758.1:c.763G>C	XP_024302526.1:p.Gly255Arg
NM_000883.4:c.994G>C MANE Select	NP_000874.2:p.Gly332Arg
NM_001102605.2:c.964G>C	NP_001096075.1:p.Gly322Arg
NM_001142573.2:c.739G>C	NP_001136045.1:p.Gly247Arg
NM_001142574.2:c.724G>C	NP_001136046.1:p.Gly242Arg
NM_001142575.2:c.664G>C	NP_001136047.1:p.Gly222Arg
NM_001142576.2:c.895G>C	NP_001136048.1:p.Gly299Arg
NM_001304521.2:c.787G>C	NP_001291450.1:p.Gly263Arg
NM_183243.3:c.886G>C	NP_899066.1:p.Gly296Arg