Canonical Allele Identifier: CA351993322

Gene: GLB1

Linked Data

• MyVariant Identifiers: chr3:g.33063128G>A (hg19) ; chr3:g.33021636G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.33021636G>A , CM000665.2:g.33021636G>A	GRCh38
NC_000003.11:g.33063128G>A , CM000665.1:g.33063128G>A	GRCh37
NC_000003.10:g.33038132G>A	NCBI36
NG_009005.1:g.80567C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307363.10:c.1163C>T MANE Select	ENSP00000306920.4:p.Ala388Val
ENST00000307363.9:c.1163C>T	ENSP00000306920.4:p.Ala388Val
ENST00000307377.12:c.770C>T	ENSP00000305920.8:p.Ala257Val
ENST00000399402.7:c.1073C>T	ENSP00000382333.2:p.Ala358Val
ENST00000461475.5:n.262C>T
ENST00000467571.5:n.200C>T
ENST00000473477.1:n.195C>T
ENST00000482097.5:n.538C>T
ENST00000497796.5:n.415C>T
NM_000404.2:c.1163C>T	NP_000395.2:p.Ala388Val
NM_000404.3:c.1163C>T	NP_000395.2:p.Ala388Val
NM_001079811.1:c.1073C>T	NP_001073279.1:p.Ala358Val
NM_001079811.2:c.1073C>T	NP_001073279.1:p.Ala358Val
NM_001135602.1:c.770C>T	NP_001129074.1:p.Ala257Val
NM_001135602.2:c.770C>T	NP_001129074.1:p.Ala257Val
NM_001317040.1:c.1307C>T	NP_001303969.1:p.Ala436Val
XR_001740634.1:n.1543-552G>A
NM_000404.4:c.1163C>T MANE Select	NP_000395.3:p.Ala388Val
NM_001079811.3:c.1073C>T	NP_001073279.2:p.Ala358Val
NM_001135602.3:c.770C>T	NP_001129074.2:p.Ala257Val
NM_001317040.2:c.1307C>T	NP_001303969.2:p.Ala436Val
NM_001393580.1:c.1163C>T	NP_001380509.1:p.Ala388Val