Canonical Allele Identifier: CA1742328345

Gene: IMPDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128398556T= , CM000669.2:g.128398556T=	GRCh38
NC_000007.13:g.128038610T= , CM000669.1:g.128038610T=	GRCh37
NC_000007.12:g.127825846T=	NCBI36
NG_009194.1:g.16427A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348127.11:c.824A=	ENSP00000265385.8:p.Asp275=
ENST00000484496.6:n.807A=
ENST00000338791.11:c.932A= MANE Select	ENSP00000345096.6:p.Asp311=
ENST00000648462.1:c.564A=
ENST00000338791.10:c.932A=	ENSP00000345096.6:p.Asp311=
ENST00000348127.10:c.824A=	ENSP00000265385.8:p.Asp275=
ENST00000354269.9:c.902A=	ENSP00000346219.5:p.Asp301=
ENST00000419067.6:c.833A=	ENSP00000399400.2:p.Asp278=
ENST00000468842.1:n.521A=
ENST00000469328.5:c.697A=
ENST00000470772.5:c.674A=	ENSP00000417296.1:p.Asp225=
ENST00000480861.5:c.662A=	ENSP00000420185.1:p.Asp221=
ENST00000484496.5:c.807A=	ENSP00000418742.1:n.807A=
ENST00000496200.5:c.602A=	ENSP00000420803.1:p.Asp201=
ENST00000497868.5:c.725A=	ENSP00000419609.1:p.Asp242=
ENST00000626419.2:c.674A=	ENSP00000486056.1:p.Asp225=
NM_000883.3:c.932A=	NP_000874.2:p.Asp311=
NM_001102605.1:c.902A=	NP_001096075.1:p.Asp301=
NM_001142573.1:c.677A=	NP_001136045.1:p.Asp226=
NM_001142574.1:c.662A=	NP_001136046.1:p.Asp221=
NM_001142575.1:c.602A=	NP_001136047.1:p.Asp201=
NM_001142576.1:c.833A=	NP_001136048.1:p.Asp278=
NM_001304521.1:c.725A=	NP_001291450.1:p.Asp242=
NM_183243.2:c.824A=	NP_899066.1:p.Asp275=
XM_005250314.1:c.701A=	XP_005250371.1:p.Asp234=
XM_006715967.1:c.932A=	XP_006716030.1:p.Asp311=
XM_006715968.1:c.902A=	XP_006716031.1:p.Asp301=
XM_006715969.1:c.824A=	XP_006716032.1:p.Asp275=
XM_006715970.2:c.725A=	XP_006716033.1:p.Asp242=
XM_006715971.1:c.701A=	XP_006716034.1:p.Asp234=
XM_011516156.1:c.314A=	XP_011514458.1:p.Asp105=
XM_011516157.1:c.314A=	XP_011514459.1:p.Asp105=
XM_017012172.1:c.701A=	XP_016867661.1:p.Asp234=
XM_017012173.1:c.902A=	XP_016867662.1:p.Asp301=
XM_024446755.1:c.902A=	XP_024302523.1:p.Asp301=
XM_024446756.1:c.824A=	XP_024302524.1:p.Asp275=
XM_024446757.1:c.725A=	XP_024302525.1:p.Asp242=
XM_024446758.1:c.701A=	XP_024302526.1:p.Asp234=
NM_000883.4:c.932A= MANE Select	NP_000874.2:p.Asp311=
NM_001102605.2:c.902A=	NP_001096075.1:p.Asp301=
NM_001142573.2:c.677A=	NP_001136045.1:p.Asp226=
NM_001142574.2:c.662A=	NP_001136046.1:p.Asp221=
NM_001142575.2:c.602A=	NP_001136047.1:p.Asp201=
NM_001142576.2:c.833A=	NP_001136048.1:p.Asp278=
NM_001304521.2:c.725A=	NP_001291450.1:p.Asp242=
NM_183243.3:c.824A=	NP_899066.1:p.Asp275=