Canonical Allele Identifier: CA433629507

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064147G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026714G>T , CM000665.2:g.49026714G>T	GRCh38
NC_000003.11:g.49064147G>T , CM000665.1:g.49064147G>T	GRCh37
NC_000003.10:g.49039151G>T	NCBI36
NG_012091.1:g.7729C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2832C>A	ENSP00000515567.1:p.Ala944=
ENST00000703937.1:c.*1893C>A	ENSP00000515568.1:n.*1893C>A
ENST00000326739.9:c.792C>A MANE Select	ENSP00000321584.4:p.Ala264=
ENST00000429182.6:c.792C>A	ENSP00000393525.2:p.Ala264=
ENST00000442157.2:c.717C>A	ENSP00000403502.2:p.Ala239=
ENST00000462980.2:n.1307C>A
ENST00000472328.2:n.858C>A
ENST00000491610.2:n.752C>A
ENST00000676607.1:n.1088C>A
ENST00000676627.1:n.1522C>A
ENST00000676708.1:n.2072C>A
ENST00000676864.1:n.1941C>A
ENST00000677010.1:c.828C>A	ENSP00000503089.1:p.Ala276=
ENST00000677108.1:n.2698C>A
ENST00000677168.1:n.1264C>A
ENST00000677185.1:n.1355C>A
ENST00000677205.1:n.1576C>A
ENST00000677344.1:n.2066C>A
ENST00000677480.1:c.*469C>A	ENSP00000504378.1:n.*469C>A
ENST00000677519.1:n.1502C>A
ENST00000677593.1:n.1348C>A
ENST00000677740.1:n.2297C>A
ENST00000677991.1:n.1965C>A
ENST00000678001.1:n.1285C>A
ENST00000678085.1:n.1348C>A
ENST00000678177.1:n.2641C>A
ENST00000678603.1:n.1870C>A
ENST00000678724.1:c.717C>A	ENSP00000503874.1:p.Ala239=
ENST00000678920.1:n.950C>A
ENST00000679019.1:n.1562C>A
ENST00000679117.1:c.*607C>A	ENSP00000503240.1:n.*607C>A
ENST00000679339.1:n.1633C>A
ENST00000326739.8:c.792C>A	ENSP00000321584.4:p.Ala264=
ENST00000429182.5:c.586C>A
ENST00000442157.1:c.717C>A	ENSP00000403502.1:p.Ala239=
ENST00000462980.1:n.694C>A
ENST00000491610.1:n.752C>A
NM_000884.2:c.792C>A	NP_000875.2:p.Ala264=
XM_006713128.2:c.1002C>A	XP_006713191.1:p.Ala334=
XM_006713128.3:c.1002C>A	XP_006713191.1:p.Ala334=
XM_017006349.1:c.927C>A	XP_016861838.1:p.Ala309=
XM_017006350.1:c.927C>A	XP_016861839.1:p.Ala309=
NM_000884.3:c.792C>A MANE Select	NP_000875.2:p.Ala264=