Canonical Allele Identifier: CA1363291643
Gene: IMPDH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49026736T= , CM000665.2:g.49026736T= GRCh38
NC_000003.11:g.49064169T= , CM000665.1:g.49064169T= GRCh37
NC_000003.10:g.49039173T= NCBI36
NG_012091.1:g.7707A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703936.1:c.2810A= ENSP00000515567.1:p.Lys937=
ENST00000703937.1:c.*1871A= ENSP00000515568.1:n.*1871A=
ENST00000326739.9:c.770A= MANE Select ENSP00000321584.4:p.Lys257=
ENST00000429182.6:c.770A= ENSP00000393525.2:p.Lys257=
ENST00000442157.2:c.695A= ENSP00000403502.2:p.Lys232=
ENST00000462980.2:n.1285A=
ENST00000472328.2:n.836A=
ENST00000491610.2:n.730A=
ENST00000676607.1:n.1066A=
ENST00000676627.1:n.1500A=
ENST00000676708.1:n.2050A=
ENST00000676864.1:n.1919A=
ENST00000677010.1:c.806A= ENSP00000503089.1:p.Lys269=
ENST00000677108.1:n.2676A=
ENST00000677168.1:n.1242A=
ENST00000677185.1:n.1333A=
ENST00000677205.1:n.1554A=
ENST00000677344.1:n.2044A=
ENST00000677480.1:c.*447A= ENSP00000504378.1:n.*447A=
ENST00000677519.1:n.1480A=
ENST00000677593.1:n.1326A=
ENST00000677740.1:n.2275A=
ENST00000677991.1:n.1943A=
ENST00000678001.1:n.1263A=
ENST00000678085.1:n.1326A=
ENST00000678177.1:n.2619A=
ENST00000678603.1:n.1848A=
ENST00000678724.1:c.695A= ENSP00000503874.1:p.Lys232=
ENST00000678920.1:n.928A=
ENST00000679019.1:n.1540A=
ENST00000679117.1:c.*585A= ENSP00000503240.1:n.*585A=
ENST00000679339.1:n.1611A=
ENST00000326739.8:c.770A= ENSP00000321584.4:p.Lys257=
ENST00000429182.5:c.564A=
ENST00000442157.1:c.695A= ENSP00000403502.1:p.Lys232=
ENST00000462980.1:n.672A=
ENST00000491610.1:n.730A=
NM_000884.2:c.770A= NP_000875.2:p.Lys257=
XM_006713128.2:c.980A= XP_006713191.1:p.Lys327=
XM_006713128.3:c.980A= XP_006713191.1:p.Lys327=
XM_017006349.1:c.905A= XP_016861838.1:p.Lys302=
XM_017006350.1:c.905A= XP_016861839.1:p.Lys302=
NM_000884.3:c.770A= MANE Select NP_000875.2:p.Lys257=