Canonical Allele Identifier: CA433629328

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064010G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026577G>T , CM000665.2:g.49026577G>T	GRCh38
NC_000003.11:g.49064010G>T , CM000665.1:g.49064010G>T	GRCh37
NC_000003.10:g.49039014G>T	NCBI36
NG_012091.1:g.7866C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000703936.1:c.2892C>A	ENSP00000515567.1:p.Ile964=
ENST00000703937.1:c.*1953C>A	ENSP00000515568.1:n.*1953C>A
ENST00000326739.9:c.852C>A MANE Select	ENSP00000321584.4:p.Ile284=
ENST00000429182.6:c.852C>A	ENSP00000393525.2:p.Ile284=
ENST00000442157.2:c.777C>A	ENSP00000403502.2:p.Ile259=
ENST00000462980.2:n.1367C>A
ENST00000472328.2:n.918C>A
ENST00000491610.2:n.812C>A
ENST00000676607.1:n.1148C>A
ENST00000676627.1:n.1582C>A
ENST00000676708.1:n.2132C>A
ENST00000676864.1:n.2001C>A
ENST00000677010.1:c.876C>A	ENSP00000503089.1:p.Ile292=
ENST00000677108.1:n.2835C>A
ENST00000677168.1:n.1324C>A
ENST00000677185.1:n.1415C>A
ENST00000677205.1:n.1636C>A
ENST00000677344.1:n.2126C>A
ENST00000677480.1:c.*529C>A	ENSP00000504378.1:n.*529C>A
ENST00000677519.1:n.1562C>A
ENST00000677593.1:n.1408C>A
ENST00000677740.1:n.2357C>A
ENST00000677991.1:n.2025C>A
ENST00000678001.1:n.1345C>A
ENST00000678085.1:n.1485C>A
ENST00000678177.1:n.2778C>A
ENST00000678603.1:n.1930C>A
ENST00000678724.1:c.777C>A	ENSP00000503874.1:p.Ile259=
ENST00000678920.1:n.1010C>A
ENST00000679019.1:n.1699C>A
ENST00000679117.1:c.*667C>A	ENSP00000503240.1:n.*667C>A
ENST00000679339.1:n.1693C>A
ENST00000326739.8:c.852C>A	ENSP00000321584.4:p.Ile284=
ENST00000429182.5:c.646C>A
ENST00000442157.1:c.777C>A	ENSP00000403502.1:p.Ile259=
ENST00000462980.1:n.754C>A
ENST00000491610.1:n.812C>A
NM_000884.2:c.852C>A	NP_000875.2:p.Ile284=
XM_006713128.2:c.1062C>A	XP_006713191.1:p.Ile354=
XM_006713128.3:c.1062C>A	XP_006713191.1:p.Ile354=
XM_017006349.1:c.987C>A	XP_016861838.1:p.Ile329=
XM_017006350.1:c.987C>A	XP_016861839.1:p.Ile329=
NM_000884.3:c.852C>A MANE Select	NP_000875.2:p.Ile284=