Canonical Allele Identifier: CA433629728

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064315C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026882C>T , CM000665.2:g.49026882C>T	GRCh38
NC_000003.11:g.49064315C>T , CM000665.1:g.49064315C>T	GRCh37
NC_000003.10:g.49039319C>T	NCBI36
NG_012091.1:g.7561G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2664G>A	ENSP00000515567.1:p.Lys888=
ENST00000703937.1:c.*1725G>A	ENSP00000515568.1:n.*1725G>A
ENST00000326739.9:c.624G>A MANE Select	ENSP00000321584.4:p.Lys208=
ENST00000429182.6:c.624G>A	ENSP00000393525.2:p.Lys208=
ENST00000442157.2:c.549G>A	ENSP00000403502.2:p.Lys183=
ENST00000462980.2:n.1139G>A
ENST00000472328.2:n.690G>A
ENST00000491610.2:n.584G>A
ENST00000676607.1:n.920G>A
ENST00000676627.1:n.1354G>A
ENST00000676708.1:n.1904G>A
ENST00000676864.1:n.1773G>A
ENST00000677010.1:c.660G>A	ENSP00000503089.1:p.Lys220=
ENST00000677108.1:n.2530G>A
ENST00000677168.1:n.1096G>A
ENST00000677185.1:n.1187G>A
ENST00000677205.1:n.1408G>A
ENST00000677344.1:n.1898G>A
ENST00000677480.1:c.*301G>A	ENSP00000504378.1:n.*301G>A
ENST00000677519.1:n.1334G>A
ENST00000677593.1:n.1180G>A
ENST00000677740.1:n.2129G>A
ENST00000677991.1:n.1797G>A
ENST00000678001.1:n.1117G>A
ENST00000678085.1:n.1180G>A
ENST00000678177.1:n.2473G>A
ENST00000678603.1:n.1702G>A
ENST00000678724.1:c.549G>A	ENSP00000503874.1:p.Lys183=
ENST00000678920.1:n.782G>A
ENST00000679019.1:n.1394G>A
ENST00000679117.1:c.*439G>A	ENSP00000503240.1:n.*439G>A
ENST00000679339.1:n.1465G>A
ENST00000326739.8:c.624G>A	ENSP00000321584.4:p.Lys208=
ENST00000429182.5:c.418G>A
ENST00000442157.1:c.549G>A	ENSP00000403502.1:p.Lys183=
ENST00000462980.1:n.526G>A
ENST00000491610.1:n.584G>A
NM_000884.2:c.624G>A	NP_000875.2:p.Lys208=
XM_006713128.2:c.834G>A	XP_006713191.1:p.Lys278=
XM_006713128.3:c.834G>A	XP_006713191.1:p.Lys278=
XM_017006349.1:c.759G>A	XP_016861838.1:p.Lys253=
XM_017006350.1:c.759G>A	XP_016861839.1:p.Lys253=
NM_000884.3:c.624G>A MANE Select	NP_000875.2:p.Lys208=