Canonical Allele Identifier: CA369169188

Gene: IMPDH1

Linked Data

• dbSNP Id: rs1584728146
• MyVariant Identifiers: chr7:g.128038589T>G (hg19) ; chr7:g.128398535T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128398535T>G , CM000669.2:g.128398535T>G	GRCh38
NC_000007.13:g.128038589T>G , CM000669.1:g.128038589T>G	GRCh37
NC_000007.12:g.127825825T>G	NCBI36
NG_009194.1:g.16448A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348127.11:c.845A>C	ENSP00000265385.8:p.Tyr282Ser
ENST00000484496.6:n.828A>C
ENST00000338791.11:c.953A>C MANE Select	ENSP00000345096.6:p.Tyr318Ser
ENST00000648462.1:c.585A>C
ENST00000338791.10:c.953A>C	ENSP00000345096.6:p.Tyr318Ser
ENST00000348127.10:c.845A>C	ENSP00000265385.8:p.Tyr282Ser
ENST00000354269.9:c.923A>C	ENSP00000346219.5:p.Tyr308Ser
ENST00000419067.6:c.854A>C	ENSP00000399400.2:p.Tyr285Ser
ENST00000468842.1:n.542A>C
ENST00000469328.5:c.718A>C
ENST00000470772.5:c.695A>C	ENSP00000417296.1:p.Tyr232Ser
ENST00000480861.5:c.683A>C	ENSP00000420185.1:p.Tyr228Ser
ENST00000484496.5:c.828A>C	ENSP00000418742.1:n.828A>C
ENST00000496200.5:c.623A>C	ENSP00000420803.1:p.Tyr208Ser
ENST00000497868.5:c.746A>C	ENSP00000419609.1:p.Tyr249Ser
ENST00000626419.2:c.695A>C	ENSP00000486056.1:p.Tyr232Ser
NM_000883.3:c.953A>C	NP_000874.2:p.Tyr318Ser
NM_001102605.1:c.923A>C	NP_001096075.1:p.Tyr308Ser
NM_001142573.1:c.698A>C	NP_001136045.1:p.Tyr233Ser
NM_001142574.1:c.683A>C	NP_001136046.1:p.Tyr228Ser
NM_001142575.1:c.623A>C	NP_001136047.1:p.Tyr208Ser
NM_001142576.1:c.854A>C	NP_001136048.1:p.Tyr285Ser
NM_001304521.1:c.746A>C	NP_001291450.1:p.Tyr249Ser
NM_183243.2:c.845A>C	NP_899066.1:p.Tyr282Ser
XM_005250314.1:c.722A>C	XP_005250371.1:p.Tyr241Ser
XM_006715967.1:c.953A>C	XP_006716030.1:p.Tyr318Ser
XM_006715968.1:c.923A>C	XP_006716031.1:p.Tyr308Ser
XM_006715969.1:c.845A>C	XP_006716032.1:p.Tyr282Ser
XM_006715970.2:c.746A>C	XP_006716033.1:p.Tyr249Ser
XM_006715971.1:c.722A>C	XP_006716034.1:p.Tyr241Ser
XM_011516156.1:c.335A>C	XP_011514458.1:p.Tyr112Ser
XM_011516157.1:c.335A>C	XP_011514459.1:p.Tyr112Ser
XM_017012172.1:c.722A>C	XP_016867661.1:p.Tyr241Ser
XM_017012173.1:c.923A>C	XP_016867662.1:p.Tyr308Ser
XM_024446755.1:c.923A>C	XP_024302523.1:p.Tyr308Ser
XM_024446756.1:c.845A>C	XP_024302524.1:p.Tyr282Ser
XM_024446757.1:c.746A>C	XP_024302525.1:p.Tyr249Ser
XM_024446758.1:c.722A>C	XP_024302526.1:p.Tyr241Ser
NM_000883.4:c.953A>C MANE Select	NP_000874.2:p.Tyr318Ser
NM_001102605.2:c.923A>C	NP_001096075.1:p.Tyr308Ser
NM_001142573.2:c.698A>C	NP_001136045.1:p.Tyr233Ser
NM_001142574.2:c.683A>C	NP_001136046.1:p.Tyr228Ser
NM_001142575.2:c.623A>C	NP_001136047.1:p.Tyr208Ser
NM_001142576.2:c.854A>C	NP_001136048.1:p.Tyr285Ser
NM_001304521.2:c.746A>C	NP_001291450.1:p.Tyr249Ser
NM_183243.3:c.845A>C	NP_899066.1:p.Tyr282Ser