Canonical Allele Identifier: CA352740772

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064262T>G (hg19) ; chr3:g.49026829T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026829T>G , CM000665.2:g.49026829T>G	GRCh38
NC_000003.11:g.49064262T>G , CM000665.1:g.49064262T>G	GRCh37
NC_000003.10:g.49039266T>G	NCBI36
NG_012091.1:g.7614A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2717A>C	ENSP00000515567.1:p.Asp906Ala
ENST00000703937.1:c.*1778A>C	ENSP00000515568.1:n.*1778A>C
ENST00000326739.9:c.677A>C MANE Select	ENSP00000321584.4:p.Asp226Ala
ENST00000429182.6:c.677A>C	ENSP00000393525.2:p.Asp226Ala
ENST00000442157.2:c.602A>C	ENSP00000403502.2:p.Asp201Ala
ENST00000462980.2:n.1192A>C
ENST00000472328.2:n.743A>C
ENST00000491610.2:n.637A>C
ENST00000676607.1:n.973A>C
ENST00000676627.1:n.1407A>C
ENST00000676708.1:n.1957A>C
ENST00000676864.1:n.1826A>C
ENST00000677010.1:c.713A>C	ENSP00000503089.1:p.Asp238Ala
ENST00000677108.1:n.2583A>C
ENST00000677168.1:n.1149A>C
ENST00000677185.1:n.1240A>C
ENST00000677205.1:n.1461A>C
ENST00000677344.1:n.1951A>C
ENST00000677480.1:c.*354A>C	ENSP00000504378.1:n.*354A>C
ENST00000677519.1:n.1387A>C
ENST00000677593.1:n.1233A>C
ENST00000677740.1:n.2182A>C
ENST00000677991.1:n.1850A>C
ENST00000678001.1:n.1170A>C
ENST00000678085.1:n.1233A>C
ENST00000678177.1:n.2526A>C
ENST00000678603.1:n.1755A>C
ENST00000678724.1:c.602A>C	ENSP00000503874.1:p.Asp201Ala
ENST00000678920.1:n.835A>C
ENST00000679019.1:n.1447A>C
ENST00000679117.1:c.*492A>C	ENSP00000503240.1:n.*492A>C
ENST00000679339.1:n.1518A>C
ENST00000326739.8:c.677A>C	ENSP00000321584.4:p.Asp226Ala
ENST00000429182.5:c.471A>C
ENST00000442157.1:c.602A>C	ENSP00000403502.1:p.Asp201Ala
ENST00000462980.1:n.579A>C
ENST00000491610.1:n.637A>C
NM_000884.2:c.677A>C	NP_000875.2:p.Asp226Ala
XM_006713128.2:c.887A>C	XP_006713191.1:p.Asp296Ala
XM_006713128.3:c.887A>C	XP_006713191.1:p.Asp296Ala
XM_017006349.1:c.812A>C	XP_016861838.1:p.Asp271Ala
XM_017006350.1:c.812A>C	XP_016861839.1:p.Asp271Ala
NM_000884.3:c.677A>C MANE Select	NP_000875.2:p.Asp226Ala