Canonical Allele Identifier: CA351988841
Community Standard Title: NM_000404.4(GLB1):c.1441G>T (p.Gly481Ter)
Gene: GLB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.33016747C>A , CM000665.2:g.33016747C>A GRCh38
NC_000003.11:g.33058239C>A , CM000665.1:g.33058239C>A GRCh37
NC_000003.10:g.33033243C>A NCBI36
NG_009005.1:g.85456G>T

Transcript Alleles

HGVS Amino-acid Change
NM_000404.4:c.1441G>T MANE Select NP_000395.3:p.Gly481Ter
ENST00000307363.10:c.1441G>T MANE Select ENSP00000306920.4:p.Gly481Ter
NM_000404.2:c.1441G>T NP_000395.2:p.Gly481Ter
NM_000404.3:c.1441G>T NP_000395.2:p.Gly481Ter
NM_001079811.1:c.1351G>T NP_001073279.1:p.Gly451Ter
NM_001079811.2:c.1351G>T NP_001073279.1:p.Gly451Ter
NM_001079811.3:c.1351G>T NP_001073279.2:p.Gly451Ter
NM_001135602.1:c.1048G>T NP_001129074.1:p.Gly350Ter
NM_001135602.2:c.1048G>T NP_001129074.1:p.Gly350Ter
NM_001135602.3:c.1048G>T NP_001129074.2:p.Gly350Ter
NM_001317040.1:c.1585G>T NP_001303969.1:p.Gly529Ter
NM_001317040.2:c.1585G>T NP_001303969.2:p.Gly529Ter
NM_001393580.1:c.1441G>T NP_001380509.1:p.Gly481Ter
ENST00000307363.9:c.1441G>T ENSP00000306920.4:p.Gly481Ter
ENST00000307377.12:c.1048G>T ENSP00000305920.8:p.Gly350Ter
ENST00000399402.7:c.1351G>T ENSP00000382333.2:p.Gly451Ter
ENST00000461475.5:n.540G>T
ENST00000467571.5:n.478G>T
ENST00000497796.5:n.693G>T