Canonical Allele Identifier: CA352741124

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064302T>C (hg19) ; chr3:g.49026869T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026869T>C , CM000665.2:g.49026869T>C	GRCh38
NC_000003.11:g.49064302T>C , CM000665.1:g.49064302T>C	GRCh37
NC_000003.10:g.49039306T>C	NCBI36
NG_012091.1:g.7574A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2677A>G	ENSP00000515567.1:p.Asn893Asp
ENST00000703937.1:c.*1738A>G	ENSP00000515568.1:n.*1738A>G
ENST00000326739.9:c.637A>G MANE Select	ENSP00000321584.4:p.Asn213Asp
ENST00000429182.6:c.637A>G	ENSP00000393525.2:p.Asn213Asp
ENST00000442157.2:c.562A>G	ENSP00000403502.2:p.Asn188Asp
ENST00000462980.2:n.1152A>G
ENST00000472328.2:n.703A>G
ENST00000491610.2:n.597A>G
ENST00000676607.1:n.933A>G
ENST00000676627.1:n.1367A>G
ENST00000676708.1:n.1917A>G
ENST00000676864.1:n.1786A>G
ENST00000677010.1:c.673A>G	ENSP00000503089.1:p.Asn225Asp
ENST00000677108.1:n.2543A>G
ENST00000677168.1:n.1109A>G
ENST00000677185.1:n.1200A>G
ENST00000677205.1:n.1421A>G
ENST00000677344.1:n.1911A>G
ENST00000677480.1:c.*314A>G	ENSP00000504378.1:n.*314A>G
ENST00000677519.1:n.1347A>G
ENST00000677593.1:n.1193A>G
ENST00000677740.1:n.2142A>G
ENST00000677991.1:n.1810A>G
ENST00000678001.1:n.1130A>G
ENST00000678085.1:n.1193A>G
ENST00000678177.1:n.2486A>G
ENST00000678603.1:n.1715A>G
ENST00000678724.1:c.562A>G	ENSP00000503874.1:p.Asn188Asp
ENST00000678920.1:n.795A>G
ENST00000679019.1:n.1407A>G
ENST00000679117.1:c.*452A>G	ENSP00000503240.1:n.*452A>G
ENST00000679339.1:n.1478A>G
ENST00000326739.8:c.637A>G	ENSP00000321584.4:p.Asn213Asp
ENST00000429182.5:c.431A>G
ENST00000442157.1:c.562A>G	ENSP00000403502.1:p.Asn188Asp
ENST00000462980.1:n.539A>G
ENST00000491610.1:n.597A>G
NM_000884.2:c.637A>G	NP_000875.2:p.Asn213Asp
XM_006713128.2:c.847A>G	XP_006713191.1:p.Asn283Asp
XM_006713128.3:c.847A>G	XP_006713191.1:p.Asn283Asp
XM_017006349.1:c.772A>G	XP_016861838.1:p.Asn258Asp
XM_017006350.1:c.772A>G	XP_016861839.1:p.Asn258Asp
NM_000884.3:c.637A>G MANE Select	NP_000875.2:p.Asn213Asp