Canonical Allele Identifier: CA352740027

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064165A>T (hg19) ; chr3:g.49026732A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026732A>T , CM000665.2:g.49026732A>T	GRCh38
NC_000003.11:g.49064165A>T , CM000665.1:g.49064165A>T	GRCh37
NC_000003.10:g.49039169A>T	NCBI36
NG_012091.1:g.7711T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2814T>A	ENSP00000515567.1:p.Tyr938Ter
ENST00000703937.1:c.*1875T>A	ENSP00000515568.1:n.*1875T>A
ENST00000326739.9:c.774T>A MANE Select	ENSP00000321584.4:p.Tyr258Ter
ENST00000429182.6:c.774T>A	ENSP00000393525.2:p.Tyr258Ter
ENST00000442157.2:c.699T>A	ENSP00000403502.2:p.Tyr233Ter
ENST00000462980.2:n.1289T>A
ENST00000472328.2:n.840T>A
ENST00000491610.2:n.734T>A
ENST00000676607.1:n.1070T>A
ENST00000676627.1:n.1504T>A
ENST00000676708.1:n.2054T>A
ENST00000676864.1:n.1923T>A
ENST00000677010.1:c.810T>A	ENSP00000503089.1:p.Tyr270Ter
ENST00000677108.1:n.2680T>A
ENST00000677168.1:n.1246T>A
ENST00000677185.1:n.1337T>A
ENST00000677205.1:n.1558T>A
ENST00000677344.1:n.2048T>A
ENST00000677480.1:c.*451T>A	ENSP00000504378.1:n.*451T>A
ENST00000677519.1:n.1484T>A
ENST00000677593.1:n.1330T>A
ENST00000677740.1:n.2279T>A
ENST00000677991.1:n.1947T>A
ENST00000678001.1:n.1267T>A
ENST00000678085.1:n.1330T>A
ENST00000678177.1:n.2623T>A
ENST00000678603.1:n.1852T>A
ENST00000678724.1:c.699T>A	ENSP00000503874.1:p.Tyr233Ter
ENST00000678920.1:n.932T>A
ENST00000679019.1:n.1544T>A
ENST00000679117.1:c.*589T>A	ENSP00000503240.1:n.*589T>A
ENST00000679339.1:n.1615T>A
ENST00000326739.8:c.774T>A	ENSP00000321584.4:p.Tyr258Ter
ENST00000429182.5:c.568T>A
ENST00000442157.1:c.699T>A	ENSP00000403502.1:p.Tyr233Ter
ENST00000462980.1:n.676T>A
ENST00000491610.1:n.734T>A
NM_000884.2:c.774T>A	NP_000875.2:p.Tyr258Ter
XM_006713128.2:c.984T>A	XP_006713191.1:p.Tyr328Ter
XM_006713128.3:c.984T>A	XP_006713191.1:p.Tyr328Ter
XM_017006349.1:c.909T>A	XP_016861838.1:p.Tyr303Ter
XM_017006350.1:c.909T>A	XP_016861839.1:p.Tyr303Ter
NM_000884.3:c.774T>A MANE Select	NP_000875.2:p.Tyr258Ter