Canonical Allele Identifier: CA369167894

Gene: IMPDH1

Linked Data

• MyVariant Identifiers: chr7:g.128038487C>A (hg19) ; chr7:g.128398433C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128398433C>A , CM000669.2:g.128398433C>A	GRCh38
NC_000007.13:g.128038487C>A , CM000669.1:g.128038487C>A	GRCh37
NC_000007.12:g.127825723C>A	NCBI36
NG_009194.1:g.16550G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348127.11:c.947G>T	ENSP00000265385.8:p.Gly316Val
ENST00000484496.6:n.930G>T
ENST00000338791.11:c.1055G>T MANE Select	ENSP00000345096.6:p.Gly352Val
ENST00000648462.1:c.687G>T
ENST00000338791.10:c.1055G>T	ENSP00000345096.6:p.Gly352Val
ENST00000348127.10:c.947G>T	ENSP00000265385.8:p.Gly316Val
ENST00000354269.9:c.1025G>T	ENSP00000346219.5:p.Gly342Val
ENST00000419067.6:c.956G>T	ENSP00000399400.2:p.Gly319Val
ENST00000469328.5:c.820G>T
ENST00000470772.5:c.797G>T	ENSP00000417296.1:p.Gly266Val
ENST00000480861.5:c.785G>T	ENSP00000420185.1:p.Gly262Val
ENST00000484496.5:c.930G>T	ENSP00000418742.1:n.930G>T
ENST00000496200.5:c.725G>T	ENSP00000420803.1:p.Gly242Val
ENST00000497868.5:c.848G>T	ENSP00000419609.1:p.Gly283Val
ENST00000626419.2:c.797G>T	ENSP00000486056.1:p.Gly266Val
NM_000883.3:c.1055G>T	NP_000874.2:p.Gly352Val
NM_001102605.1:c.1025G>T	NP_001096075.1:p.Gly342Val
NM_001142573.1:c.800G>T	NP_001136045.1:p.Gly267Val
NM_001142574.1:c.785G>T	NP_001136046.1:p.Gly262Val
NM_001142575.1:c.725G>T	NP_001136047.1:p.Gly242Val
NM_001142576.1:c.956G>T	NP_001136048.1:p.Gly319Val
NM_001304521.1:c.848G>T	NP_001291450.1:p.Gly283Val
NM_183243.2:c.947G>T	NP_899066.1:p.Gly316Val
XM_005250314.1:c.824G>T	XP_005250371.1:p.Gly275Val
XM_006715967.1:c.1055G>T	XP_006716030.1:p.Gly352Val
XM_006715968.1:c.1025G>T	XP_006716031.1:p.Gly342Val
XM_006715969.1:c.947G>T	XP_006716032.1:p.Gly316Val
XM_006715970.2:c.848G>T	XP_006716033.1:p.Gly283Val
XM_006715971.1:c.824G>T	XP_006716034.1:p.Gly275Val
XM_011516156.1:c.437G>T	XP_011514458.1:p.Gly146Val
XM_011516157.1:c.437G>T	XP_011514459.1:p.Gly146Val
XM_017012172.1:c.824G>T	XP_016867661.1:p.Gly275Val
XM_017012173.1:c.1025G>T	XP_016867662.1:p.Gly342Val
XM_024446755.1:c.1025G>T	XP_024302523.1:p.Gly342Val
XM_024446756.1:c.947G>T	XP_024302524.1:p.Gly316Val
XM_024446757.1:c.848G>T	XP_024302525.1:p.Gly283Val
XM_024446758.1:c.824G>T	XP_024302526.1:p.Gly275Val
NM_000883.4:c.1055G>T MANE Select	NP_000874.2:p.Gly352Val
NM_001102605.2:c.1025G>T	NP_001096075.1:p.Gly342Val
NM_001142573.2:c.800G>T	NP_001136045.1:p.Gly267Val
NM_001142574.2:c.785G>T	NP_001136046.1:p.Gly262Val
NM_001142575.2:c.725G>T	NP_001136047.1:p.Gly242Val
NM_001142576.2:c.956G>T	NP_001136048.1:p.Gly319Val
NM_001304521.2:c.848G>T	NP_001291450.1:p.Gly283Val
NM_183243.3:c.947G>T	NP_899066.1:p.Gly316Val