Canonical Allele Identifier: CA352740896

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064284C>T (hg19) ; chr3:g.49026851C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026851C>T , CM000665.2:g.49026851C>T	GRCh38
NC_000003.11:g.49064284C>T , CM000665.1:g.49064284C>T	GRCh37
NC_000003.10:g.49039288C>T	NCBI36
NG_012091.1:g.7592G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2695G>A	ENSP00000515567.1:p.Val899Met
ENST00000703937.1:c.*1756G>A	ENSP00000515568.1:n.*1756G>A
ENST00000326739.9:c.655G>A MANE Select	ENSP00000321584.4:p.Val219Met
ENST00000429182.6:c.655G>A	ENSP00000393525.2:p.Val219Met
ENST00000442157.2:c.580G>A	ENSP00000403502.2:p.Val194Met
ENST00000462980.2:n.1170G>A
ENST00000472328.2:n.721G>A
ENST00000491610.2:n.615G>A
ENST00000676607.1:n.951G>A
ENST00000676627.1:n.1385G>A
ENST00000676708.1:n.1935G>A
ENST00000676864.1:n.1804G>A
ENST00000677010.1:c.691G>A	ENSP00000503089.1:p.Val231Met
ENST00000677108.1:n.2561G>A
ENST00000677168.1:n.1127G>A
ENST00000677185.1:n.1218G>A
ENST00000677205.1:n.1439G>A
ENST00000677344.1:n.1929G>A
ENST00000677480.1:c.*332G>A	ENSP00000504378.1:n.*332G>A
ENST00000677519.1:n.1365G>A
ENST00000677593.1:n.1211G>A
ENST00000677740.1:n.2160G>A
ENST00000677991.1:n.1828G>A
ENST00000678001.1:n.1148G>A
ENST00000678085.1:n.1211G>A
ENST00000678177.1:n.2504G>A
ENST00000678603.1:n.1733G>A
ENST00000678724.1:c.580G>A	ENSP00000503874.1:p.Val194Met
ENST00000678920.1:n.813G>A
ENST00000679019.1:n.1425G>A
ENST00000679117.1:c.*470G>A	ENSP00000503240.1:n.*470G>A
ENST00000679339.1:n.1496G>A
ENST00000326739.8:c.655G>A	ENSP00000321584.4:p.Val219Met
ENST00000429182.5:c.449G>A
ENST00000442157.1:c.580G>A	ENSP00000403502.1:p.Val194Met
ENST00000462980.1:n.557G>A
ENST00000491610.1:n.615G>A
NM_000884.2:c.655G>A	NP_000875.2:p.Val219Met
XM_006713128.2:c.865G>A	XP_006713191.1:p.Val289Met
XM_006713128.3:c.865G>A	XP_006713191.1:p.Val289Met
XM_017006349.1:c.790G>A	XP_016861838.1:p.Val264Met
XM_017006350.1:c.790G>A	XP_016861839.1:p.Val264Met
NM_000884.3:c.655G>A MANE Select	NP_000875.2:p.Val219Met