Canonical Allele Identifier: CA352740957

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064292T>C (hg19) ; chr3:g.49026859T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026859T>C , CM000665.2:g.49026859T>C	GRCh38
NC_000003.11:g.49064292T>C , CM000665.1:g.49064292T>C	GRCh37
NC_000003.10:g.49039296T>C	NCBI36
NG_012091.1:g.7584A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2687A>G	ENSP00000515567.1:p.Asp896Gly
ENST00000703937.1:c.*1748A>G	ENSP00000515568.1:n.*1748A>G
ENST00000326739.9:c.647A>G MANE Select	ENSP00000321584.4:p.Asp216Gly
ENST00000429182.6:c.647A>G	ENSP00000393525.2:p.Asp216Gly
ENST00000442157.2:c.572A>G	ENSP00000403502.2:p.Asp191Gly
ENST00000462980.2:n.1162A>G
ENST00000472328.2:n.713A>G
ENST00000491610.2:n.607A>G
ENST00000676607.1:n.943A>G
ENST00000676627.1:n.1377A>G
ENST00000676708.1:n.1927A>G
ENST00000676864.1:n.1796A>G
ENST00000677010.1:c.683A>G	ENSP00000503089.1:p.Asp228Gly
ENST00000677108.1:n.2553A>G
ENST00000677168.1:n.1119A>G
ENST00000677185.1:n.1210A>G
ENST00000677205.1:n.1431A>G
ENST00000677344.1:n.1921A>G
ENST00000677480.1:c.*324A>G	ENSP00000504378.1:n.*324A>G
ENST00000677519.1:n.1357A>G
ENST00000677593.1:n.1203A>G
ENST00000677740.1:n.2152A>G
ENST00000677991.1:n.1820A>G
ENST00000678001.1:n.1140A>G
ENST00000678085.1:n.1203A>G
ENST00000678177.1:n.2496A>G
ENST00000678603.1:n.1725A>G
ENST00000678724.1:c.572A>G	ENSP00000503874.1:p.Asp191Gly
ENST00000678920.1:n.805A>G
ENST00000679019.1:n.1417A>G
ENST00000679117.1:c.*462A>G	ENSP00000503240.1:n.*462A>G
ENST00000679339.1:n.1488A>G
ENST00000326739.8:c.647A>G	ENSP00000321584.4:p.Asp216Gly
ENST00000429182.5:c.441A>G
ENST00000442157.1:c.572A>G	ENSP00000403502.1:p.Asp191Gly
ENST00000462980.1:n.549A>G
ENST00000491610.1:n.607A>G
NM_000884.2:c.647A>G	NP_000875.2:p.Asp216Gly
XM_006713128.2:c.857A>G	XP_006713191.1:p.Asp286Gly
XM_006713128.3:c.857A>G	XP_006713191.1:p.Asp286Gly
XM_017006349.1:c.782A>G	XP_016861838.1:p.Asp261Gly
XM_017006350.1:c.782A>G	XP_016861839.1:p.Asp261Gly
NM_000884.3:c.647A>G MANE Select	NP_000875.2:p.Asp216Gly