Canonical Allele Identifier: CA352001622
Community Standard Title: NM_000404.4(GLB1):c.818G>A (p.Trp273Ter)
Gene: GLB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.33051979C>T , CM000665.2:g.33051979C>T GRCh38
NC_000003.11:g.33093471C>T , CM000665.1:g.33093471C>T GRCh37
NC_000003.10:g.33068475C>T NCBI36
NG_009005.1:g.50224G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000404.4:c.818G>A MANE Select NP_000395.3:p.Trp273Ter
ENST00000307363.10:c.818G>A MANE Select ENSP00000306920.4:p.Trp273Ter
NM_000404.2:c.818G>A NP_000395.2:p.Trp273Ter
NM_000404.3:c.818G>A NP_000395.2:p.Trp273Ter
NM_001079811.1:c.728G>A NP_001073279.1:p.Trp243Ter
NM_001079811.2:c.728G>A NP_001073279.1:p.Trp243Ter
NM_001079811.3:c.728G>A NP_001073279.2:p.Trp243Ter
NM_001135602.1:c.425G>A NP_001129074.1:p.Trp142Ter
NM_001135602.2:c.425G>A NP_001129074.1:p.Trp142Ter
NM_001135602.3:c.425G>A NP_001129074.2:p.Trp142Ter
NM_001317040.1:c.962G>A NP_001303969.1:p.Trp321Ter
NM_001317040.2:c.962G>A NP_001303969.2:p.Trp321Ter
NM_001393580.1:c.818G>A NP_001380509.1:p.Trp273Ter
ENST00000307363.9:c.818G>A ENSP00000306920.4:p.Trp273Ter
ENST00000307377.12:c.425G>A ENSP00000305920.8:p.Trp142Ter
ENST00000399402.7:c.728G>A ENSP00000382333.2:p.Trp243Ter
ENST00000415454.1:c.341G>A ENSP00000411813.1:p.Trp114Ter
ENST00000438227.1:c.*310G>A ENSP00000401250.1:n.*310G>A
ENST00000446732.5:c.*261G>A ENSP00000407365.1:n.*261G>A
ENST00000482097.5:n.193G>A
ENST00000485698.5:n.221G>A
ENST00000498537.5:n.344G>A