Canonical Allele Identifier: CA2536936844

Gene: IMPDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128400836_128400838del , CM000669.2:g.128400836_128400838del	GRCh38
NC_000007.13:g.128040890_128040892del , CM000669.1:g.128040890_128040892del	GRCh37
NC_000007.12:g.127828126_127828128del	NCBI36
NG_009194.1:g.14146_14148del

Transcript Alleles

HGVS	Amino-acid change
ENST00000348127.11:c.451_453del	ENSP00000265385.8:p.Asn151del
ENST00000484496.6:n.415_417del
ENST00000338791.11:c.559_561del MANE Select	ENSP00000345096.6:p.Asn187del
ENST00000648462.1:c.206_208del
ENST00000338791.10:c.559_561del	ENSP00000345096.6:p.Asn187del
ENST00000348127.10:c.451_453del	ENSP00000265385.8:p.Asn151del
ENST00000354269.9:c.529_531del	ENSP00000346219.5:p.Asn177del
ENST00000419067.6:c.460_462del	ENSP00000399400.2:p.Asn154del
ENST00000469328.5:c.305_307del
ENST00000470772.5:c.304_306del	ENSP00000417296.1:p.Asn102del
ENST00000480861.5:c.304_306del	ENSP00000420185.1:p.Asn102del
ENST00000484496.5:c.415_417del	ENSP00000418742.1:p.Asn139del
ENST00000489263.1:c.297+178_297+180del	ENSP00000418592.1:n.297+178_297+180del
ENST00000491376.5:n.728_730del
ENST00000496200.5:c.249+178_249+180del	ENSP00000420803.1:n.249+178_249+180del
ENST00000496487.5:n.379_381del
ENST00000497868.5:c.352_354del	ENSP00000419609.1:p.Asn118del
ENST00000626419.2:c.304_306del	ENSP00000486056.1:p.Asn102del
NM_000883.3:c.559_561del	NP_000874.2:p.Asn187del
NM_001102605.1:c.529_531del	NP_001096075.1:p.Asn177del
NM_001142573.1:c.304_306del	NP_001136045.1:p.Asn102del
NM_001142574.1:c.304_306del	NP_001136046.1:p.Asn102del
NM_001142575.1:c.249+178_249+180del	NP_001136047.1:n.249+178_249+180del
NM_001142576.1:c.460_462del	NP_001136048.1:p.Asn154del
NM_001304521.1:c.352_354del	NP_001291450.1:p.Asn118del
NM_183243.2:c.451_453del	NP_899066.1:p.Asn151del
XM_005250314.1:c.328_330del	XP_005250371.1:p.Asn110del
XM_006715967.1:c.559_561del	XP_006716030.1:p.Asn187del
XM_006715968.1:c.529_531del	XP_006716031.1:p.Asn177del
XM_006715969.1:c.451_453del	XP_006716032.1:p.Asn151del
XM_006715970.2:c.352_354del	XP_006716033.1:p.Asn118del
XM_006715971.1:c.328_330del	XP_006716034.1:p.Asn110del
XM_017012172.1:c.328_330del	XP_016867661.1:p.Asn110del
XM_017012173.1:c.529_531del	XP_016867662.1:p.Asn177del
XM_024446755.1:c.529_531del	XP_024302523.1:p.Asn177del
XM_024446756.1:c.451_453del	XP_024302524.1:p.Asn151del
XM_024446757.1:c.352_354del	XP_024302525.1:p.Asn118del
XM_024446758.1:c.328_330del	XP_024302526.1:p.Asn110del
NM_000883.4:c.559_561del MANE Select	NP_000874.2:p.Asn187del
NM_001102605.2:c.529_531del	NP_001096075.1:p.Asn177del
NM_001142573.2:c.304_306del	NP_001136045.1:p.Asn102del
NM_001142574.2:c.304_306del	NP_001136046.1:p.Asn102del
NM_001142575.2:c.249+178_249+180del	NP_001136047.1:n.249+178_249+180del
NM_001142576.2:c.460_462del	NP_001136048.1:p.Asn154del
NM_001304521.2:c.352_354del	NP_001291450.1:p.Asn118del
NM_183243.3:c.451_453del	NP_899066.1:p.Asn151del