Canonical Allele Identifier: CA352830640
Community Standard Title: NM_021971.4(GMPPB):c.191T>G (p.Met64Arg)
Gene: GMPPB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49723411A>C , CM000665.2:g.49723411A>C GRCh38
NC_000003.11:g.49760844A>C , CM000665.1:g.49760844A>C GRCh37
NC_000003.10:g.49735848A>C NCBI36
NG_011603.1:g.38855A>C
NG_033731.1:g.5564T>G
NG_033731.2:g.5564T>G

Transcript Alleles

HGVS Amino-acid Change
NM_021971.4:c.191T>G MANE Select NP_068806.2:p.Met64Arg
ENST00000308388.7:c.191T>G MANE Select ENSP00000311130.6:p.Met64Arg
NM_013334.3:c.191T>G NP_037466.2:p.Met64Arg
NM_013334.4:c.191T>G NP_037466.3:p.Met64Arg
NM_021971.2:c.191T>G NP_068806.1:p.Met64Arg
ENST00000308375.10:c.191T>G ENSP00000309092.6:p.Met64Arg
ENST00000308388.6:c.191T>G ENSP00000311130.6:p.Met64Arg
ENST00000480687.5:c.191T>G ENSP00000418565.1:p.Met64Arg
ENST00000481959.1:n.404T>G
ENST00000481959.2:n.408T>G
ENST00000495627.1:n.381T>G
ENST00000495627.2:c.191T>G ENSP00000503768.1:p.Met64Arg
ENST00000677393.1:c.191T>G ENSP00000503880.1:p.Met64Arg
ENST00000678010.1:c.191T>G ENSP00000503176.1:p.Met64Arg
ENST00000678208.1:n.408T>G
ENST00000678853.1:c.191T>G ENSP00000504692.1:p.Met64Arg