Canonical Allele Identifier: CA351993261

Gene: GLB1

Linked Data

• MyVariant Identifiers: chr3:g.33063118A>C (hg19) ; chr3:g.33021626A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.33021626A>C , CM000665.2:g.33021626A>C	GRCh38
NC_000003.11:g.33063118A>C , CM000665.1:g.33063118A>C	GRCh37
NC_000003.10:g.33038122A>C	NCBI36
NG_009005.1:g.80577T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307363.10:c.1173T>G MANE Select	ENSP00000306920.4:p.Ile391Met
ENST00000307363.9:c.1173T>G	ENSP00000306920.4:p.Ile391Met
ENST00000307377.12:c.780T>G	ENSP00000305920.8:p.Ile260Met
ENST00000399402.7:c.1083T>G	ENSP00000382333.2:p.Ile361Met
ENST00000461475.5:n.272T>G
ENST00000467571.5:n.210T>G
ENST00000473477.1:n.205T>G
ENST00000497796.5:n.425T>G
NM_000404.2:c.1173T>G	NP_000395.2:p.Ile391Met
NM_000404.3:c.1173T>G	NP_000395.2:p.Ile391Met
NM_001079811.1:c.1083T>G	NP_001073279.1:p.Ile361Met
NM_001079811.2:c.1083T>G	NP_001073279.1:p.Ile361Met
NM_001135602.1:c.780T>G	NP_001129074.1:p.Ile260Met
NM_001135602.2:c.780T>G	NP_001129074.1:p.Ile260Met
NM_001317040.1:c.1317T>G	NP_001303969.1:p.Ile439Met
XR_001740634.1:n.1543-562A>C
NM_000404.4:c.1173T>G MANE Select	NP_000395.3:p.Ile391Met
NM_001079811.3:c.1083T>G	NP_001073279.2:p.Ile361Met
NM_001135602.3:c.780T>G	NP_001129074.2:p.Ile260Met
NM_001317040.2:c.1317T>G	NP_001303969.2:p.Ile439Met
NM_001393580.1:c.1173T>G	NP_001380509.1:p.Ile391Met