Canonical Allele Identifier: CA352740163

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064184G>T (hg19) ; chr3:g.49026751G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026751G>T , CM000665.2:g.49026751G>T	GRCh38
NC_000003.11:g.49064184G>T , CM000665.1:g.49064184G>T	GRCh37
NC_000003.10:g.49039188G>T	NCBI36
NG_012091.1:g.7692C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2795C>A	ENSP00000515567.1:p.Thr932Asn
ENST00000703937.1:c.*1856C>A	ENSP00000515568.1:n.*1856C>A
ENST00000326739.9:c.755C>A MANE Select	ENSP00000321584.4:p.Thr252Asn
ENST00000429182.6:c.755C>A	ENSP00000393525.2:p.Thr252Asn
ENST00000442157.2:c.680C>A	ENSP00000403502.2:p.Thr227Asn
ENST00000462980.2:n.1270C>A
ENST00000472328.2:n.821C>A
ENST00000491610.2:n.715C>A
ENST00000676607.1:n.1051C>A
ENST00000676627.1:n.1485C>A
ENST00000676708.1:n.2035C>A
ENST00000676864.1:n.1904C>A
ENST00000677010.1:c.791C>A	ENSP00000503089.1:p.Thr264Asn
ENST00000677108.1:n.2661C>A
ENST00000677168.1:n.1227C>A
ENST00000677185.1:n.1318C>A
ENST00000677205.1:n.1539C>A
ENST00000677344.1:n.2029C>A
ENST00000677480.1:c.*432C>A	ENSP00000504378.1:n.*432C>A
ENST00000677519.1:n.1465C>A
ENST00000677593.1:n.1311C>A
ENST00000677740.1:n.2260C>A
ENST00000677991.1:n.1928C>A
ENST00000678001.1:n.1248C>A
ENST00000678085.1:n.1311C>A
ENST00000678177.1:n.2604C>A
ENST00000678603.1:n.1833C>A
ENST00000678724.1:c.680C>A	ENSP00000503874.1:p.Thr227Asn
ENST00000678920.1:n.913C>A
ENST00000679019.1:n.1525C>A
ENST00000679117.1:c.*570C>A	ENSP00000503240.1:n.*570C>A
ENST00000679339.1:n.1596C>A
ENST00000326739.8:c.755C>A	ENSP00000321584.4:p.Thr252Asn
ENST00000429182.5:c.549C>A
ENST00000442157.1:c.680C>A	ENSP00000403502.1:p.Thr227Asn
ENST00000462980.1:n.657C>A
ENST00000491610.1:n.715C>A
NM_000884.2:c.755C>A	NP_000875.2:p.Thr252Asn
XM_006713128.2:c.965C>A	XP_006713191.1:p.Thr322Asn
XM_006713128.3:c.965C>A	XP_006713191.1:p.Thr322Asn
XM_017006349.1:c.890C>A	XP_016861838.1:p.Thr297Asn
XM_017006350.1:c.890C>A	XP_016861839.1:p.Thr297Asn
NM_000884.3:c.755C>A MANE Select	NP_000875.2:p.Thr252Asn