Canonical Allele Identifier: CA833102800

Gene: IMPDH1

Linked Data

• dbSNP Id: rs1404119677
• MyVariant Identifiers: chr7:g.128041125_128041127del (hg19) ; chr7:g.128401071_128401073del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128401072_128401074del , CM000669.2:g.128401072_128401074del	GRCh38
NC_000007.13:g.128041126_128041128del , CM000669.1:g.128041126_128041128del	GRCh37
NC_000007.12:g.127828362_127828364del	NCBI36
NG_009194.1:g.13910_13912del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348127.11:c.338_340del	ENSP00000265385.8:p.Pro113del
ENST00000484496.6:n.302_304del
ENST00000338791.11:c.446_448del MANE Select	ENSP00000345096.6:p.Pro149del
ENST00000648462.1:c.93_95del
ENST00000338791.10:c.446_448del	ENSP00000345096.6:p.Pro149del
ENST00000348127.10:c.338_340del	ENSP00000265385.8:p.Pro113del
ENST00000354269.9:c.416_418del	ENSP00000346219.5:p.Pro139del
ENST00000419067.6:c.347_349del	ENSP00000399400.2:p.Pro116del
ENST00000469328.5:c.192_194del
ENST00000470772.5:c.191_193del	ENSP00000417296.1:p.Pro64del
ENST00000473463.1:c.*192_*194del	ENSP00000420469.1:n.*192_*194del
ENST00000480861.5:c.191_193del	ENSP00000420185.1:p.Pro64del
ENST00000484496.5:c.302_304del	ENSP00000418742.1:p.Pro101del
ENST00000489263.1:c.239_241del	ENSP00000418592.1:p.Pro80del
ENST00000491376.5:n.615_617del
ENST00000496200.5:c.191_193del	ENSP00000420803.1:p.Pro64del
ENST00000496487.5:n.266_268del
ENST00000497868.5:c.239_241del	ENSP00000419609.1:p.Pro80del
ENST00000626419.2:c.191_193del	ENSP00000486056.1:p.Pro64del
NM_000883.3:c.446_448del	NP_000874.2:p.Pro149del
NM_001102605.1:c.416_418del	NP_001096075.1:p.Pro139del
NM_001142573.1:c.191_193del	NP_001136045.1:p.Pro64del
NM_001142574.1:c.191_193del	NP_001136046.1:p.Pro64del
NM_001142575.1:c.191_193del	NP_001136047.1:p.Pro64del
NM_001142576.1:c.347_349del	NP_001136048.1:p.Pro116del
NM_001304521.1:c.239_241del	NP_001291450.1:p.Pro80del
NM_183243.2:c.338_340del	NP_899066.1:p.Pro113del
XM_005250314.1:c.215_217del	XP_005250371.1:p.Pro72del
XM_006715967.1:c.446_448del	XP_006716030.1:p.Pro149del
XM_006715968.1:c.416_418del	XP_006716031.1:p.Pro139del
XM_006715969.1:c.338_340del	XP_006716032.1:p.Pro113del
XM_006715970.2:c.239_241del	XP_006716033.1:p.Pro80del
XM_006715971.1:c.215_217del	XP_006716034.1:p.Pro72del
XM_017012172.1:c.215_217del	XP_016867661.1:p.Pro72del
XM_017012173.1:c.416_418del	XP_016867662.1:p.Pro139del
XM_024446755.1:c.416_418del	XP_024302523.1:p.Pro139del
XM_024446756.1:c.338_340del	XP_024302524.1:p.Pro113del
XM_024446757.1:c.239_241del	XP_024302525.1:p.Pro80del
XM_024446758.1:c.215_217del	XP_024302526.1:p.Pro72del
NM_000883.4:c.446_448del MANE Select	NP_000874.2:p.Pro149del
NM_001102605.2:c.416_418del	NP_001096075.1:p.Pro139del
NM_001142573.2:c.191_193del	NP_001136045.1:p.Pro64del
NM_001142574.2:c.191_193del	NP_001136046.1:p.Pro64del
NM_001142575.2:c.191_193del	NP_001136047.1:p.Pro64del
NM_001142576.2:c.347_349del	NP_001136048.1:p.Pro116del
NM_001304521.2:c.239_241del	NP_001291450.1:p.Pro80del
NM_183243.3:c.338_340del	NP_899066.1:p.Pro113del