Canonical Allele Identifier: CA2299521

Gene: GLB1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.33046156A>G , CM000665.2:g.33046156A>G	GRCh38
NC_000003.11:g.33087648A>G , CM000665.1:g.33087648A>G	GRCh37
NC_000003.10:g.33062652A>G	NCBI36
NG_009005.1:g.56047T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000404.4:c.1032T>C MANE Select	NP_000395.3:p.Thr344=
ENST00000307363.10:c.1032T>C MANE Select	ENSP00000306920.4:p.Thr344=
NM_000404.2:c.1032T>C	NP_000395.2:p.Thr344=
NM_000404.3:c.1032T>C	NP_000395.2:p.Thr344=
NM_001079811.1:c.942T>C	NP_001073279.1:p.Thr314=
NM_001079811.2:c.942T>C	NP_001073279.1:p.Thr314=
NM_001079811.3:c.942T>C	NP_001073279.2:p.Thr314=
NM_001135602.1:c.639T>C	NP_001129074.1:p.Thr213=
NM_001135602.2:c.639T>C	NP_001129074.1:p.Thr213=
NM_001135602.3:c.639T>C	NP_001129074.2:p.Thr213=
NM_001317040.1:c.1176T>C	NP_001303969.1:p.Thr392=
NM_001317040.2:c.1176T>C	NP_001303969.2:p.Thr392=
NM_001393580.1:c.1032T>C	NP_001380509.1:p.Thr344=
ENST00000307363.9:c.1032T>C	ENSP00000306920.4:p.Thr344=
ENST00000307377.12:c.639T>C	ENSP00000305920.8:p.Thr213=
ENST00000399402.7:c.942T>C	ENSP00000382333.2:p.Thr314=
ENST00000415454.1:c.555T>C	ENSP00000411813.1:p.Thr185=
ENST00000482097.5:n.407T>C
ENST00000485698.5:n.435T>C
ENST00000490658.2:n.37T>C
ENST00000498537.5:n.558T>C