Canonical Allele Identifier: CA1355976925

Gene: GLB1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.32997169G= , CM000665.2:g.32997169G=	GRCh38
NC_000003.11:g.33038661G= , CM000665.1:g.33038661G=	GRCh37
NC_000003.10:g.33013665G=	NCBI36
NG_009005.1:g.105034C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307363.10:c.1910C= MANE Select	ENSP00000306920.4:p.Thr637=
ENST00000307363.9:c.1910C=	ENSP00000306920.4:p.Thr637=
ENST00000307377.12:c.1517C=	ENSP00000305920.8:p.Thr506=
ENST00000399402.7:c.1820C=	ENSP00000382333.2:p.Thr607=
NM_000404.2:c.1910C=	NP_000395.2:p.Thr637=
NM_000404.3:c.1910C=	NP_000395.2:p.Thr637=
NM_001079811.1:c.1820C=	NP_001073279.1:p.Thr607=
NM_001079811.2:c.1820C=	NP_001073279.1:p.Thr607=
NM_001135602.1:c.1517C=	NP_001129074.1:p.Thr506=
NM_001135602.2:c.1517C=	NP_001129074.1:p.Thr506=
NM_001317040.1:c.2054C=	NP_001303969.1:p.Thr685=
NM_000404.4:c.1910C= MANE Select	NP_000395.3:p.Thr637=
NM_001079811.3:c.1820C=	NP_001073279.2:p.Thr607=
NM_001135602.3:c.1517C=	NP_001129074.2:p.Thr506=
NM_001317040.2:c.2054C=	NP_001303969.2:p.Thr685=
NM_001393580.1:c.1734+16887C=	NP_001380509.1:n.1734+16887C=