Canonical Allele Identifier: CA12638770

Gene: IMPDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128409647T>A , CM000669.2:g.128409647T>A	GRCh38
NC_000007.13:g.128049701T>A , CM000669.1:g.128049701T>A	GRCh37
NC_000007.12:g.127836937T>A	NCBI36
NG_009194.1:g.5336A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348127.11:c.146+109A>T	ENSP00000265385.8:n.146+109A>T
ENST00000338791.11:c.146+109A>T MANE Select	ENSP00000345096.6:n.146+109A>T
ENST00000338791.10:c.146+109A>T	ENSP00000345096.6:n.146+109A>T
ENST00000348127.10:c.146+109A>T	ENSP00000265385.8:n.146+109A>T
ENST00000354269.9:c.146+109A>T	ENSP00000346219.5:n.146+109A>T
ENST00000419067.6:c.146+109A>T	ENSP00000399400.2:n.146+109A>T
ENST00000473463.1:c.146+109A>T	ENSP00000420469.1:n.146+109A>T
ENST00000489263.1:c.146+109A>T	ENSP00000418592.1:n.146+109A>T
ENST00000491376.5:n.227+109A>T
ENST00000497868.5:c.146+109A>T	ENSP00000419609.1:n.146+109A>T
ENST00000626419.2:c.-110+109A>T	ENSP00000486056.1:n.-110+109A>T
NM_000883.3:c.146+109A>T	NP_000874.2:n.146+109A>T
NM_001102605.1:c.146+109A>T	NP_001096075.1:n.146+109A>T
NM_001142576.1:c.146+109A>T	NP_001136048.1:n.146+109A>T
NM_001304521.1:c.146+109A>T	NP_001291450.1:n.146+109A>T
NM_183243.2:c.146+109A>T	NP_899066.1:n.146+109A>T
XM_005250314.1:c.-42+109A>T	XP_005250371.1:n.-42+109A>T
XM_006715967.1:c.146+109A>T	XP_006716030.1:n.146+109A>T
XM_006715968.1:c.146+109A>T	XP_006716031.1:n.146+109A>T
XM_006715969.1:c.146+109A>T	XP_006716032.1:n.146+109A>T
XM_006715970.2:c.146+109A>T	XP_006716033.1:n.146+109A>T
XM_006715971.1:c.-42+109A>T	XP_006716034.1:n.-42+109A>T
XM_017012172.1:c.-174+109A>T	XP_016867661.1:n.-174+109A>T
XM_017012173.1:c.146+109A>T	XP_016867662.1:n.146+109A>T
XM_024446755.1:c.146+109A>T	XP_024302523.1:n.146+109A>T
XM_024446756.1:c.146+109A>T	XP_024302524.1:n.146+109A>T
XM_024446757.1:c.146+109A>T	XP_024302525.1:n.146+109A>T
XM_024446758.1:c.-174+109A>T	XP_024302526.1:n.-174+109A>T
NM_000883.4:c.146+109A>T MANE Select	NP_000874.2:n.146+109A>T
NM_001102605.2:c.146+109A>T	NP_001096075.1:n.146+109A>T
NM_001142576.2:c.146+109A>T	NP_001136048.1:n.146+109A>T
NM_001304521.2:c.146+109A>T	NP_001291450.1:n.146+109A>T
NM_183243.3:c.146+109A>T	NP_899066.1:n.146+109A>T