Canonical Allele Identifier: CA433629512

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064156G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026723G>A , CM000665.2:g.49026723G>A	GRCh38
NC_000003.11:g.49064156G>A , CM000665.1:g.49064156G>A	GRCh37
NC_000003.10:g.49039160G>A	NCBI36
NG_012091.1:g.7720C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2823C>T	ENSP00000515567.1:p.Asp941=
ENST00000703937.1:c.*1884C>T	ENSP00000515568.1:n.*1884C>T
ENST00000326739.9:c.783C>T MANE Select	ENSP00000321584.4:p.Asp261=
ENST00000429182.6:c.783C>T	ENSP00000393525.2:p.Asp261=
ENST00000442157.2:c.708C>T	ENSP00000403502.2:p.Asp236=
ENST00000462980.2:n.1298C>T
ENST00000472328.2:n.849C>T
ENST00000491610.2:n.743C>T
ENST00000676607.1:n.1079C>T
ENST00000676627.1:n.1513C>T
ENST00000676708.1:n.2063C>T
ENST00000676864.1:n.1932C>T
ENST00000677010.1:c.819C>T	ENSP00000503089.1:p.Asp273=
ENST00000677108.1:n.2689C>T
ENST00000677168.1:n.1255C>T
ENST00000677185.1:n.1346C>T
ENST00000677205.1:n.1567C>T
ENST00000677344.1:n.2057C>T
ENST00000677480.1:c.*460C>T	ENSP00000504378.1:n.*460C>T
ENST00000677519.1:n.1493C>T
ENST00000677593.1:n.1339C>T
ENST00000677740.1:n.2288C>T
ENST00000677991.1:n.1956C>T
ENST00000678001.1:n.1276C>T
ENST00000678085.1:n.1339C>T
ENST00000678177.1:n.2632C>T
ENST00000678603.1:n.1861C>T
ENST00000678724.1:c.708C>T	ENSP00000503874.1:p.Asp236=
ENST00000678920.1:n.941C>T
ENST00000679019.1:n.1553C>T
ENST00000679117.1:c.*598C>T	ENSP00000503240.1:n.*598C>T
ENST00000679339.1:n.1624C>T
ENST00000326739.8:c.783C>T	ENSP00000321584.4:p.Asp261=
ENST00000429182.5:c.577C>T
ENST00000442157.1:c.708C>T	ENSP00000403502.1:p.Asp236=
ENST00000462980.1:n.685C>T
ENST00000491610.1:n.743C>T
NM_000884.2:c.783C>T	NP_000875.2:p.Asp261=
XM_006713128.2:c.993C>T	XP_006713191.1:p.Asp331=
XM_006713128.3:c.993C>T	XP_006713191.1:p.Asp331=
XM_017006349.1:c.918C>T	XP_016861838.1:p.Asp306=
XM_017006350.1:c.918C>T	XP_016861839.1:p.Asp306=
NM_000884.3:c.783C>T MANE Select	NP_000875.2:p.Asp261=