Canonical Allele Identifier: CA352831442
Community Standard Title: NM_021971.4(GMPPB):c.94C>T (p.Pro32Ser)
Gene: GMPPB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49723633G>A , CM000665.2:g.49723633G>A GRCh38
NC_000003.11:g.49761066G>A , CM000665.1:g.49761066G>A GRCh37
NC_000003.10:g.49736070G>A NCBI36
NG_033731.1:g.5342C>T
NG_033731.2:g.5342C>T

Transcript Alleles

HGVS Amino-acid Change
NM_021971.4:c.94C>T MANE Select NP_068806.2:p.Pro32Ser
ENST00000308388.7:c.94C>T MANE Select ENSP00000311130.6:p.Pro32Ser
NM_013334.3:c.94C>T NP_037466.2:p.Pro32Ser
NM_013334.4:c.94C>T NP_037466.3:p.Pro32Ser
NM_021971.2:c.94C>T NP_068806.1:p.Pro32Ser
ENST00000308375.10:c.94C>T ENSP00000309092.6:p.Pro32Ser
ENST00000308388.6:c.94C>T ENSP00000311130.6:p.Pro32Ser
ENST00000480687.5:c.94C>T ENSP00000418565.1:p.Pro32Ser
ENST00000481959.1:n.311C>T
ENST00000481959.2:n.311C>T
ENST00000495627.1:n.284C>T
ENST00000495627.2:c.94C>T ENSP00000503768.1:p.Pro32Ser
ENST00000677393.1:c.94C>T ENSP00000503880.1:p.Pro32Ser
ENST00000678010.1:c.94C>T ENSP00000503176.1:p.Pro32Ser
ENST00000678208.1:n.311C>T
ENST00000678853.1:c.94C>T ENSP00000504692.1:p.Pro32Ser