Canonical Allele Identifier: CA433554453

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064400G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026967G>A , CM000665.2:g.49026967G>A	GRCh38
NC_000003.11:g.49064400G>A , CM000665.1:g.49064400G>A	GRCh37
NC_000003.10:g.49039404G>A	NCBI36
NG_012091.1:g.7476C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2652C>T	ENSP00000515567.1:p.Ser884=
ENST00000703937.1:c.*1713C>T	ENSP00000515568.1:n.*1713C>T
ENST00000326739.9:c.612C>T MANE Select	ENSP00000321584.4:p.Ser204=
ENST00000429182.6:c.612C>T	ENSP00000393525.2:p.Ser204=
ENST00000442157.2:c.537C>T	ENSP00000403502.2:p.Ser179=
ENST00000462980.2:n.1127C>T
ENST00000472328.2:n.678C>T
ENST00000491610.2:n.499C>T
ENST00000676607.1:n.908C>T
ENST00000676627.1:n.1342C>T
ENST00000676708.1:n.1819C>T
ENST00000676864.1:n.1688C>T
ENST00000677010.1:c.648C>T	ENSP00000503089.1:p.Ser216=
ENST00000677108.1:n.2445C>T
ENST00000677168.1:n.1084C>T
ENST00000677185.1:n.1102C>T
ENST00000677205.1:n.1323C>T
ENST00000677344.1:n.1813C>T
ENST00000677480.1:c.*289C>T	ENSP00000504378.1:n.*289C>T
ENST00000677519.1:n.1322C>T
ENST00000677593.1:n.1095C>T
ENST00000677740.1:n.2044C>T
ENST00000677991.1:n.1785C>T
ENST00000678001.1:n.1105C>T
ENST00000678085.1:n.1095C>T
ENST00000678177.1:n.2388C>T
ENST00000678603.1:n.1690C>T
ENST00000678724.1:c.537C>T	ENSP00000503874.1:p.Ser179=
ENST00000678920.1:n.770C>T
ENST00000679019.1:n.1309C>T
ENST00000679117.1:c.*427C>T	ENSP00000503240.1:n.*427C>T
ENST00000679339.1:n.1380C>T
ENST00000326739.8:c.612C>T	ENSP00000321584.4:p.Ser204=
ENST00000429182.5:c.406C>T
ENST00000442157.1:c.537C>T	ENSP00000403502.1:p.Ser179=
ENST00000462980.1:n.514C>T
ENST00000491610.1:n.499C>T
NM_000884.2:c.612C>T	NP_000875.2:p.Ser204=
XM_006713128.2:c.822C>T	XP_006713191.1:p.Ser274=
XM_006713128.3:c.822C>T	XP_006713191.1:p.Ser274=
XM_017006349.1:c.747C>T	XP_016861838.1:p.Ser249=
XM_017006350.1:c.747C>T	XP_016861839.1:p.Ser249=
NM_000884.3:c.612C>T MANE Select	NP_000875.2:p.Ser204=