Canonical Allele Identifier: CA352826008

Gene: GMPPB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49721799G>A , CM000665.2:g.49721799G>A	GRCh38
NC_000003.11:g.49759232G>A , CM000665.1:g.49759232G>A	GRCh37
NC_000003.10:g.49734236G>A	NCBI36
NG_011603.1:g.37243G>A
NG_033731.1:g.7176C>T
NG_033731.2:g.7176C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_021971.4:c.1036C>T MANE Select	NP_068806.2:p.His346Tyr
ENST00000308388.7:c.1036C>T MANE Select	ENSP00000311130.6:p.His346Tyr
NM_013334.3:c.1117C>T	NP_037466.2:p.His373Tyr
NM_013334.4:c.1117C>T	NP_037466.3:p.His373Tyr
NM_021971.2:c.1036C>T	NP_068806.1:p.His346Tyr
ENST00000308375.10:c.1117C>T	ENSP00000309092.6:p.His373Tyr
ENST00000308388.6:c.1036C>T	ENSP00000311130.6:p.His346Tyr
ENST00000480687.5:c.1036C>T	ENSP00000418565.1:p.His346Tyr
ENST00000481959.2:n.1609C>T
ENST00000495627.2:c.1144C>T	ENSP00000503768.1:p.His382Tyr
ENST00000677393.1:c.*53C>T	ENSP00000503880.1:n.*53C>T
ENST00000678010.1:c.670C>T	ENSP00000503176.1:p.His224Tyr
ENST00000678208.1:n.1470C>T
ENST00000678853.1:c.*327C>T	ENSP00000504692.1:n.*327C>T