Canonical Allele Identifier: CA433554507

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064421T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026988T>C , CM000665.2:g.49026988T>C	GRCh38
NC_000003.11:g.49064421T>C , CM000665.1:g.49064421T>C	GRCh37
NC_000003.10:g.49039425T>C	NCBI36
NG_012091.1:g.7455A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2631A>G	ENSP00000515567.1:p.Ala877=
ENST00000703937.1:c.*1692A>G	ENSP00000515568.1:n.*1692A>G
ENST00000326739.9:c.591A>G MANE Select	ENSP00000321584.4:p.Ala197=
ENST00000429182.6:c.591A>G	ENSP00000393525.2:p.Ala197=
ENST00000442157.2:c.516A>G	ENSP00000403502.2:p.Ala172=
ENST00000462980.2:n.1106A>G
ENST00000472328.2:n.657A>G
ENST00000491610.2:n.478A>G
ENST00000676607.1:n.887A>G
ENST00000676627.1:n.1321A>G
ENST00000676708.1:n.1798A>G
ENST00000676864.1:n.1667A>G
ENST00000677010.1:c.627A>G	ENSP00000503089.1:p.Ala209=
ENST00000677108.1:n.2424A>G
ENST00000677168.1:n.1063A>G
ENST00000677185.1:n.1081A>G
ENST00000677205.1:n.1302A>G
ENST00000677344.1:n.1792A>G
ENST00000677480.1:c.*268A>G	ENSP00000504378.1:n.*268A>G
ENST00000677519.1:n.1301A>G
ENST00000677593.1:n.1074A>G
ENST00000677740.1:n.2023A>G
ENST00000677991.1:n.1764A>G
ENST00000678001.1:n.1084A>G
ENST00000678085.1:n.1074A>G
ENST00000678177.1:n.2367A>G
ENST00000678603.1:n.1669A>G
ENST00000678724.1:c.516A>G	ENSP00000503874.1:p.Ala172=
ENST00000678920.1:n.749A>G
ENST00000679019.1:n.1288A>G
ENST00000679117.1:c.*406A>G	ENSP00000503240.1:n.*406A>G
ENST00000679339.1:n.1359A>G
ENST00000326739.8:c.591A>G	ENSP00000321584.4:p.Ala197=
ENST00000429182.5:c.385A>G
ENST00000442157.1:c.516A>G	ENSP00000403502.1:p.Ala172=
ENST00000462980.1:n.493A>G
ENST00000491610.1:n.478A>G
NM_000884.2:c.591A>G	NP_000875.2:p.Ala197=
XM_006713128.2:c.801A>G	XP_006713191.1:p.Ala267=
XM_006713128.3:c.801A>G	XP_006713191.1:p.Ala267=
XM_017006349.1:c.726A>G	XP_016861838.1:p.Ala242=
XM_017006350.1:c.726A>G	XP_016861839.1:p.Ala242=
NM_000884.3:c.591A>G MANE Select	NP_000875.2:p.Ala197=