Canonical Allele Identifier: CA352740734

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064256T>A (hg19) ; chr3:g.49026823T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026823T>A , CM000665.2:g.49026823T>A	GRCh38
NC_000003.11:g.49064256T>A , CM000665.1:g.49064256T>A	GRCh37
NC_000003.10:g.49039260T>A	NCBI36
NG_012091.1:g.7620A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2723A>T	ENSP00000515567.1:p.Lys908Met
ENST00000703937.1:c.*1784A>T	ENSP00000515568.1:n.*1784A>T
ENST00000326739.9:c.683A>T MANE Select	ENSP00000321584.4:p.Lys228Met
ENST00000429182.6:c.683A>T	ENSP00000393525.2:p.Lys228Met
ENST00000442157.2:c.608A>T	ENSP00000403502.2:p.Lys203Met
ENST00000462980.2:n.1198A>T
ENST00000472328.2:n.749A>T
ENST00000491610.2:n.643A>T
ENST00000676607.1:n.979A>T
ENST00000676627.1:n.1413A>T
ENST00000676708.1:n.1963A>T
ENST00000676864.1:n.1832A>T
ENST00000677010.1:c.719A>T	ENSP00000503089.1:p.Lys240Met
ENST00000677108.1:n.2589A>T
ENST00000677168.1:n.1155A>T
ENST00000677185.1:n.1246A>T
ENST00000677205.1:n.1467A>T
ENST00000677344.1:n.1957A>T
ENST00000677480.1:c.*360A>T	ENSP00000504378.1:n.*360A>T
ENST00000677519.1:n.1393A>T
ENST00000677593.1:n.1239A>T
ENST00000677740.1:n.2188A>T
ENST00000677991.1:n.1856A>T
ENST00000678001.1:n.1176A>T
ENST00000678085.1:n.1239A>T
ENST00000678177.1:n.2532A>T
ENST00000678603.1:n.1761A>T
ENST00000678724.1:c.608A>T	ENSP00000503874.1:p.Lys203Met
ENST00000678920.1:n.841A>T
ENST00000679019.1:n.1453A>T
ENST00000679117.1:c.*498A>T	ENSP00000503240.1:n.*498A>T
ENST00000679339.1:n.1524A>T
ENST00000326739.8:c.683A>T	ENSP00000321584.4:p.Lys228Met
ENST00000429182.5:c.477A>T
ENST00000442157.1:c.608A>T	ENSP00000403502.1:p.Lys203Met
ENST00000462980.1:n.585A>T
ENST00000491610.1:n.643A>T
NM_000884.2:c.683A>T	NP_000875.2:p.Lys228Met
XM_006713128.2:c.893A>T	XP_006713191.1:p.Lys298Met
XM_006713128.3:c.893A>T	XP_006713191.1:p.Lys298Met
XM_017006349.1:c.818A>T	XP_016861838.1:p.Lys273Met
XM_017006350.1:c.818A>T	XP_016861839.1:p.Lys273Met
NM_000884.3:c.683A>T MANE Select	NP_000875.2:p.Lys228Met