Canonical Allele Identifier: CA432952503

Gene: GLB1

Linked Data

• MyVariant Identifiers: chr3:g.33110342G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.33068850G>T , CM000665.2:g.33068850G>T	GRCh38
NC_000003.11:g.33110342G>T , CM000665.1:g.33110342G>T	GRCh37
NC_000003.10:g.33085346G>T	NCBI36
NG_009005.1:g.33353C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307363.10:c.366C>A MANE Select	ENSP00000306920.4:p.Pro122=
ENST00000307363.9:c.366C>A	ENSP00000306920.4:p.Pro122=
ENST00000307377.12:c.246-3293C>A	ENSP00000305920.8:n.246-3293C>A
ENST00000399402.7:c.276C>A	ENSP00000382333.2:p.Pro92=
ENST00000415454.1:c.76-10581C>A	ENSP00000411813.1:n.76-10581C>A
ENST00000438227.1:c.76-3293C>A	ENSP00000401250.1:n.76-3293C>A
ENST00000440656.1:c.-28C>A	ENSP00000411769.1:n.-28C>A
ENST00000446732.5:c.156-3293C>A	ENSP00000407365.1:n.156-3293C>A
ENST00000450835.1:c.276C>A	ENSP00000403264.1:p.Pro92=
ENST00000464355.1:n.324C>A
ENST00000482097.5:n.109-15301C>A
ENST00000485698.5:n.137-15301C>A
ENST00000498537.5:n.133-15301C>A
NM_000404.2:c.366C>A	NP_000395.2:p.Pro122=
NM_000404.3:c.366C>A	NP_000395.2:p.Pro122=
NM_001079811.1:c.276C>A	NP_001073279.1:p.Pro92=
NM_001079811.2:c.276C>A	NP_001073279.1:p.Pro92=
NM_001135602.1:c.246-3293C>A	NP_001129074.1:n.246-3293C>A
NM_001135602.2:c.246-3293C>A	NP_001129074.1:n.246-3293C>A
NM_001317040.1:c.510C>A	NP_001303969.1:p.Pro170=
NM_000404.4:c.366C>A MANE Select	NP_000395.3:p.Pro122=
NM_001079811.3:c.276C>A	NP_001073279.2:p.Pro92=
NM_001135602.3:c.246-3293C>A	NP_001129074.2:n.246-3293C>A
NM_001317040.2:c.510C>A	NP_001303969.2:p.Pro170=
NM_001393580.1:c.366C>A	NP_001380509.1:p.Pro122=