Canonical Allele Identifier: CA2684775829

Gene: IMPDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128392283A>G , CM000669.2:g.128392283A>G	GRCh38
NC_000007.13:g.128032337A>G , CM000669.1:g.128032337A>G	GRCh37
NC_000007.12:g.127819573A>G	NCBI36
NG_009194.1:g.22700T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348127.11:c.*724T>C	ENSP00000265385.8:n.*724T>C
ENST00000484496.6:n.2416T>C
ENST00000338791.11:c.*724T>C MANE Select	ENSP00000345096.6:n.*724T>C
ENST00000338791.10:c.*724T>C	ENSP00000345096.6:n.*724T>C
ENST00000354269.9:c.*724T>C	ENSP00000346219.5:n.*724T>C
ENST00000419067.6:c.2425T>C	ENSP00000399400.2:n.2425T>C
ENST00000469328.5:c.2289T>C
ENST00000484496.5:c.2416T>C	ENSP00000418742.1:n.2416T>C
ENST00000496200.5:c.*724T>C	ENSP00000420803.1:n.*724T>C
NM_000883.3:c.*724T>C	NP_000874.2:n.*724T>C
NM_001102605.1:c.*724T>C	NP_001096075.1:n.*724T>C
NM_001142573.1:c.*724T>C	NP_001136045.1:n.*724T>C
NM_001142574.1:c.*724T>C	NP_001136046.1:n.*724T>C
NM_001142575.1:c.*724T>C	NP_001136047.1:n.*724T>C
NM_001142576.1:c.*724T>C	NP_001136048.1:n.*724T>C
NM_001304521.1:c.*724T>C	NP_001291450.1:n.*724T>C
NM_183243.2:c.*724T>C	NP_899066.1:n.*724T>C
XM_005250314.1:c.*724T>C	XP_005250371.1:n.*724T>C
XM_006715967.1:c.*645T>C	XP_006716030.1:n.*645T>C
XM_006715968.1:c.*645T>C	XP_006716031.1:n.*645T>C
XM_006715969.1:c.*645T>C	XP_006716032.1:n.*645T>C
XM_006715970.2:c.*645T>C	XP_006716033.1:n.*645T>C
XM_006715971.1:c.*645T>C	XP_006716034.1:n.*645T>C
XM_011516156.1:c.*645T>C	XP_011514458.1:n.*645T>C
XM_011516157.1:c.*724T>C	XP_011514459.1:n.*724T>C
NR_148338.1:n.893A>G
NR_148339.1:n.509A>G
XM_017012172.1:c.*724T>C	XP_016867661.1:n.*724T>C
XM_024446755.1:c.*645T>C	XP_024302523.1:n.*645T>C
XM_024446756.1:c.*645T>C	XP_024302524.1:n.*645T>C
XM_024446757.1:c.*645T>C	XP_024302525.1:n.*645T>C
XM_024446758.1:c.*645T>C	XP_024302526.1:n.*645T>C
NM_000883.4:c.*724T>C MANE Select	NP_000874.2:n.*724T>C
NM_001102605.2:c.*724T>C	NP_001096075.1:n.*724T>C
NM_001142573.2:c.*724T>C	NP_001136045.1:n.*724T>C
NM_001142574.2:c.*724T>C	NP_001136046.1:n.*724T>C
NM_001142575.2:c.*724T>C	NP_001136047.1:n.*724T>C
NM_001142576.2:c.*724T>C	NP_001136048.1:n.*724T>C
NM_001304521.2:c.*724T>C	NP_001291450.1:n.*724T>C
NM_183243.3:c.*724T>C	NP_899066.1:n.*724T>C