Canonical Allele Identifier: CA369174115

Gene: IMPDH1

Linked Data

• MyVariant Identifiers: chr7:g.128040894C>A (hg19) ; chr7:g.128400840C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128400840C>A , CM000669.2:g.128400840C>A	GRCh38
NC_000007.13:g.128040894C>A , CM000669.1:g.128040894C>A	GRCh37
NC_000007.12:g.127828130C>A	NCBI36
NG_009194.1:g.14143G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000348127.11:c.448G>T	ENSP00000265385.8:p.Ala150Ser
ENST00000484496.6:n.412G>T
ENST00000338791.11:c.556G>T MANE Select	ENSP00000345096.6:p.Ala186Ser
ENST00000648462.1:c.203G>T
ENST00000338791.10:c.556G>T	ENSP00000345096.6:p.Ala186Ser
ENST00000348127.10:c.448G>T	ENSP00000265385.8:p.Ala150Ser
ENST00000354269.9:c.526G>T	ENSP00000346219.5:p.Ala176Ser
ENST00000419067.6:c.457G>T	ENSP00000399400.2:p.Ala153Ser
ENST00000469328.5:c.302G>T
ENST00000470772.5:c.301G>T	ENSP00000417296.1:p.Ala101Ser
ENST00000480861.5:c.301G>T	ENSP00000420185.1:p.Ala101Ser
ENST00000484496.5:c.412G>T	ENSP00000418742.1:p.Ala138Ser
ENST00000489263.1:c.297+175G>T	ENSP00000418592.1:n.297+175G>T
ENST00000491376.5:n.725G>T
ENST00000496200.5:c.249+175G>T	ENSP00000420803.1:n.249+175G>T
ENST00000496487.5:n.376G>T
ENST00000497868.5:c.349G>T	ENSP00000419609.1:p.Ala117Ser
ENST00000626419.2:c.301G>T	ENSP00000486056.1:p.Ala101Ser
NM_000883.3:c.556G>T	NP_000874.2:p.Ala186Ser
NM_001102605.1:c.526G>T	NP_001096075.1:p.Ala176Ser
NM_001142573.1:c.301G>T	NP_001136045.1:p.Ala101Ser
NM_001142574.1:c.301G>T	NP_001136046.1:p.Ala101Ser
NM_001142575.1:c.249+175G>T	NP_001136047.1:n.249+175G>T
NM_001142576.1:c.457G>T	NP_001136048.1:p.Ala153Ser
NM_001304521.1:c.349G>T	NP_001291450.1:p.Ala117Ser
NM_183243.2:c.448G>T	NP_899066.1:p.Ala150Ser
XM_005250314.1:c.325G>T	XP_005250371.1:p.Ala109Ser
XM_006715967.1:c.556G>T	XP_006716030.1:p.Ala186Ser
XM_006715968.1:c.526G>T	XP_006716031.1:p.Ala176Ser
XM_006715969.1:c.448G>T	XP_006716032.1:p.Ala150Ser
XM_006715970.2:c.349G>T	XP_006716033.1:p.Ala117Ser
XM_006715971.1:c.325G>T	XP_006716034.1:p.Ala109Ser
XM_017012172.1:c.325G>T	XP_016867661.1:p.Ala109Ser
XM_017012173.1:c.526G>T	XP_016867662.1:p.Ala176Ser
XM_024446755.1:c.526G>T	XP_024302523.1:p.Ala176Ser
XM_024446756.1:c.448G>T	XP_024302524.1:p.Ala150Ser
XM_024446757.1:c.349G>T	XP_024302525.1:p.Ala117Ser
XM_024446758.1:c.325G>T	XP_024302526.1:p.Ala109Ser
NM_000883.4:c.556G>T MANE Select	NP_000874.2:p.Ala186Ser
NM_001102605.2:c.526G>T	NP_001096075.1:p.Ala176Ser
NM_001142573.2:c.301G>T	NP_001136045.1:p.Ala101Ser
NM_001142574.2:c.301G>T	NP_001136046.1:p.Ala101Ser
NM_001142575.2:c.249+175G>T	NP_001136047.1:n.249+175G>T
NM_001142576.2:c.457G>T	NP_001136048.1:p.Ala153Ser
NM_001304521.2:c.349G>T	NP_001291450.1:p.Ala117Ser
NM_183243.3:c.448G>T	NP_899066.1:p.Ala150Ser