Canonical Allele Identifier: CA352741638

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064408G>T (hg19) ; chr3:g.49026975G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026975G>T , CM000665.2:g.49026975G>T	GRCh38
NC_000003.11:g.49064408G>T , CM000665.1:g.49064408G>T	GRCh37
NC_000003.10:g.49039412G>T	NCBI36
NG_012091.1:g.7468C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2644C>A	ENSP00000515567.1:p.Gln882Lys
ENST00000703937.1:c.*1705C>A	ENSP00000515568.1:n.*1705C>A
ENST00000326739.9:c.604C>A MANE Select	ENSP00000321584.4:p.Gln202Lys
ENST00000429182.6:c.604C>A	ENSP00000393525.2:p.Gln202Lys
ENST00000442157.2:c.529C>A	ENSP00000403502.2:p.Gln177Lys
ENST00000462980.2:n.1119C>A
ENST00000472328.2:n.670C>A
ENST00000491610.2:n.491C>A
ENST00000676607.1:n.900C>A
ENST00000676627.1:n.1334C>A
ENST00000676708.1:n.1811C>A
ENST00000676864.1:n.1680C>A
ENST00000677010.1:c.640C>A	ENSP00000503089.1:p.Gln214Lys
ENST00000677108.1:n.2437C>A
ENST00000677168.1:n.1076C>A
ENST00000677185.1:n.1094C>A
ENST00000677205.1:n.1315C>A
ENST00000677344.1:n.1805C>A
ENST00000677480.1:c.*281C>A	ENSP00000504378.1:n.*281C>A
ENST00000677519.1:n.1314C>A
ENST00000677593.1:n.1087C>A
ENST00000677740.1:n.2036C>A
ENST00000677991.1:n.1777C>A
ENST00000678001.1:n.1097C>A
ENST00000678085.1:n.1087C>A
ENST00000678177.1:n.2380C>A
ENST00000678603.1:n.1682C>A
ENST00000678724.1:c.529C>A	ENSP00000503874.1:p.Gln177Lys
ENST00000678920.1:n.762C>A
ENST00000679019.1:n.1301C>A
ENST00000679117.1:c.*419C>A	ENSP00000503240.1:n.*419C>A
ENST00000679339.1:n.1372C>A
ENST00000326739.8:c.604C>A	ENSP00000321584.4:p.Gln202Lys
ENST00000429182.5:c.398C>A
ENST00000442157.1:c.529C>A	ENSP00000403502.1:p.Gln177Lys
ENST00000462980.1:n.506C>A
ENST00000491610.1:n.491C>A
NM_000884.2:c.604C>A	NP_000875.2:p.Gln202Lys
XM_006713128.2:c.814C>A	XP_006713191.1:p.Gln272Lys
XM_006713128.3:c.814C>A	XP_006713191.1:p.Gln272Lys
XM_017006349.1:c.739C>A	XP_016861838.1:p.Gln247Lys
XM_017006350.1:c.739C>A	XP_016861839.1:p.Gln247Lys
NM_000884.3:c.604C>A MANE Select	NP_000875.2:p.Gln202Lys