Canonical Allele Identifier: CA352827470
Community Standard Title: NM_021971.4(GMPPB):c.832G>A (p.Val278Met)
Gene: GMPPB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49722084C>T , CM000665.2:g.49722084C>T GRCh38
NC_000003.11:g.49759517C>T , CM000665.1:g.49759517C>T GRCh37
NC_000003.10:g.49734521C>T NCBI36
NG_011603.1:g.37528C>T
NG_033731.1:g.6891G>A
NG_033731.2:g.6891G>A

Transcript Alleles

HGVS Amino-acid Change
NM_021971.4:c.832G>A MANE Select NP_068806.2:p.Val278Met
ENST00000308388.7:c.832G>A MANE Select ENSP00000311130.6:p.Val278Met
NM_013334.3:c.832G>A NP_037466.2:p.Val278Met
NM_013334.4:c.832G>A NP_037466.3:p.Val278Met
NM_021971.2:c.832G>A NP_068806.1:p.Val278Met
ENST00000308375.10:c.832G>A ENSP00000309092.6:p.Val278Met
ENST00000308388.6:c.832G>A ENSP00000311130.6:p.Val278Met
ENST00000480687.5:c.832G>A ENSP00000418565.1:p.Val278Met
ENST00000481959.2:n.1405G>A
ENST00000495627.2:c.940G>A ENSP00000503768.1:p.Val314Met
ENST00000677393.1:c.625G>A ENSP00000503880.1:p.Val209Met
ENST00000678010.1:c.466G>A ENSP00000503176.1:p.Val156Met
ENST00000678208.1:n.1266G>A
ENST00000678853.1:c.*123G>A ENSP00000504692.1:n.*123G>A