Canonical Allele Identifier: CA369169153

Gene: IMPDH1

Linked Data

• MyVariant Identifiers: chr7:g.128038586G>T (hg19) ; chr7:g.128398532G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128398532G>T , CM000669.2:g.128398532G>T	GRCh38
NC_000007.13:g.128038586G>T , CM000669.1:g.128038586G>T	GRCh37
NC_000007.12:g.127825822G>T	NCBI36
NG_009194.1:g.16451C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348127.11:c.848C>A	ENSP00000265385.8:p.Pro283His
ENST00000484496.6:n.831C>A
ENST00000338791.11:c.956C>A MANE Select	ENSP00000345096.6:p.Pro319His
ENST00000648462.1:c.588C>A
ENST00000338791.10:c.956C>A	ENSP00000345096.6:p.Pro319His
ENST00000348127.10:c.848C>A	ENSP00000265385.8:p.Pro283His
ENST00000354269.9:c.926C>A	ENSP00000346219.5:p.Pro309His
ENST00000419067.6:c.857C>A	ENSP00000399400.2:p.Pro286His
ENST00000468842.1:n.545C>A
ENST00000469328.5:c.721C>A
ENST00000470772.5:c.698C>A	ENSP00000417296.1:p.Pro233His
ENST00000480861.5:c.686C>A	ENSP00000420185.1:p.Pro229His
ENST00000484496.5:c.831C>A	ENSP00000418742.1:n.831C>A
ENST00000496200.5:c.626C>A	ENSP00000420803.1:p.Pro209His
ENST00000497868.5:c.749C>A	ENSP00000419609.1:p.Pro250His
ENST00000626419.2:c.698C>A	ENSP00000486056.1:p.Pro233His
NM_000883.3:c.956C>A	NP_000874.2:p.Pro319His
NM_001102605.1:c.926C>A	NP_001096075.1:p.Pro309His
NM_001142573.1:c.701C>A	NP_001136045.1:p.Pro234His
NM_001142574.1:c.686C>A	NP_001136046.1:p.Pro229His
NM_001142575.1:c.626C>A	NP_001136047.1:p.Pro209His
NM_001142576.1:c.857C>A	NP_001136048.1:p.Pro286His
NM_001304521.1:c.749C>A	NP_001291450.1:p.Pro250His
NM_183243.2:c.848C>A	NP_899066.1:p.Pro283His
XM_005250314.1:c.725C>A	XP_005250371.1:p.Pro242His
XM_006715967.1:c.956C>A	XP_006716030.1:p.Pro319His
XM_006715968.1:c.926C>A	XP_006716031.1:p.Pro309His
XM_006715969.1:c.848C>A	XP_006716032.1:p.Pro283His
XM_006715970.2:c.749C>A	XP_006716033.1:p.Pro250His
XM_006715971.1:c.725C>A	XP_006716034.1:p.Pro242His
XM_011516156.1:c.338C>A	XP_011514458.1:p.Pro113His
XM_011516157.1:c.338C>A	XP_011514459.1:p.Pro113His
XM_017012172.1:c.725C>A	XP_016867661.1:p.Pro242His
XM_017012173.1:c.926C>A	XP_016867662.1:p.Pro309His
XM_024446755.1:c.926C>A	XP_024302523.1:p.Pro309His
XM_024446756.1:c.848C>A	XP_024302524.1:p.Pro283His
XM_024446757.1:c.749C>A	XP_024302525.1:p.Pro250His
XM_024446758.1:c.725C>A	XP_024302526.1:p.Pro242His
NM_000883.4:c.956C>A MANE Select	NP_000874.2:p.Pro319His
NM_001102605.2:c.926C>A	NP_001096075.1:p.Pro309His
NM_001142573.2:c.701C>A	NP_001136045.1:p.Pro234His
NM_001142574.2:c.686C>A	NP_001136046.1:p.Pro229His
NM_001142575.2:c.626C>A	NP_001136047.1:p.Pro209His
NM_001142576.2:c.857C>A	NP_001136048.1:p.Pro286His
NM_001304521.2:c.749C>A	NP_001291450.1:p.Pro250His
NM_183243.3:c.848C>A	NP_899066.1:p.Pro283His