Canonical Allele Identifier: CA352740260

Gene: IMPDH2

Linked Data

• dbSNP Id: rs1553736596
• MyVariant Identifiers: chr3:g.49064196_49064197insGC (hg19) ; chr3:g.49026763_49026764insGC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026763_49026764insGC , CM000665.2:g.49026763_49026764insGC	GRCh38
NC_000003.11:g.49064196_49064197insGC , CM000665.1:g.49064196_49064197insGC	GRCh37
NC_000003.10:g.49039200_49039201insGC	NCBI36
NG_012091.1:g.7679_7680insGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2782_2783insGC	ENSP00000515567.1:p.Ala928GlyfsTer24
ENST00000703937.1:c.*1843_*1844insGC	ENSP00000515568.1:n.*1843_*1844insGC
ENST00000326739.9:c.742_743insGC MANE Select	ENSP00000321584.4:p.Ala248GlyfsTer24
ENST00000429182.6:c.742_743insGC	ENSP00000393525.2:p.Ala248GlyfsTer24
ENST00000442157.2:c.667_668insGC	ENSP00000403502.2:p.Ala223GlyfsTer24
ENST00000462980.2:n.1257_1258insGC
ENST00000472328.2:n.808_809insGC
ENST00000491610.2:n.702_703insGC
ENST00000676607.1:n.1038_1039insGC
ENST00000676627.1:n.1472_1473insGC
ENST00000676708.1:n.2022_2023insGC
ENST00000676864.1:n.1891_1892insGC
ENST00000677010.1:c.778_779insGC	ENSP00000503089.1:p.Ala260GlyfsTer24
ENST00000677108.1:n.2648_2649insGC
ENST00000677168.1:n.1214_1215insGC
ENST00000677185.1:n.1305_1306insGC
ENST00000677205.1:n.1526_1527insGC
ENST00000677344.1:n.2016_2017insGC
ENST00000677480.1:c.*419_*420insGC	ENSP00000504378.1:n.*419_*420insGC
ENST00000677519.1:n.1452_1453insGC
ENST00000677593.1:n.1298_1299insGC
ENST00000677740.1:n.2247_2248insGC
ENST00000677991.1:n.1915_1916insGC
ENST00000678001.1:n.1235_1236insGC
ENST00000678085.1:n.1298_1299insGC
ENST00000678177.1:n.2591_2592insGC
ENST00000678603.1:n.1820_1821insGC
ENST00000678724.1:c.667_668insGC	ENSP00000503874.1:p.Ala223GlyfsTer24
ENST00000678920.1:n.900_901insGC
ENST00000679019.1:n.1512_1513insGC
ENST00000679117.1:c.*557_*558insGC	ENSP00000503240.1:n.*557_*558insGC
ENST00000679339.1:n.1583_1584insGC
ENST00000326739.8:c.742_743insGC	ENSP00000321584.4:p.Ala248GlyfsTer24
ENST00000429182.5:c.536_537insGC
ENST00000442157.1:c.667_668insGC	ENSP00000403502.1:p.Ala223GlyfsTer24
ENST00000462980.1:n.644_645insGC
ENST00000491610.1:n.702_703insGC
NM_000884.2:c.742_743insGC	NP_000875.2:p.Ala248GlyfsTer24
XM_006713128.2:c.952_953insGC	XP_006713191.1:p.Ala318GlyfsTer24
XM_006713128.3:c.952_953insGC	XP_006713191.1:p.Ala318GlyfsTer24
XM_017006349.1:c.877_878insGC	XP_016861838.1:p.Ala293GlyfsTer24
XM_017006350.1:c.877_878insGC	XP_016861839.1:p.Ala293GlyfsTer24
NM_000884.3:c.742_743insGC MANE Select	NP_000875.2:p.Ala248GlyfsTer24