Canonical Allele Identifier: CA351993351

Gene: GLB1

Linked Data

• MyVariant Identifiers: chr3:g.33063132C>T (hg19) ; chr3:g.33021640C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.33021640C>T , CM000665.2:g.33021640C>T	GRCh38
NC_000003.11:g.33063132C>T , CM000665.1:g.33063132C>T	GRCh37
NC_000003.10:g.33038136C>T	NCBI36
NG_009005.1:g.80563G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307363.10:c.1159G>A MANE Select	ENSP00000306920.4:p.Ala387Thr
ENST00000307363.9:c.1159G>A	ENSP00000306920.4:p.Ala387Thr
ENST00000307377.12:c.766G>A	ENSP00000305920.8:p.Ala256Thr
ENST00000399402.7:c.1069G>A	ENSP00000382333.2:p.Ala357Thr
ENST00000461475.5:n.258G>A
ENST00000467571.5:n.196G>A
ENST00000473477.1:n.191G>A
ENST00000482097.5:n.534G>A
ENST00000497796.5:n.411G>A
NM_000404.2:c.1159G>A	NP_000395.2:p.Ala387Thr
NM_000404.3:c.1159G>A	NP_000395.2:p.Ala387Thr
NM_001079811.1:c.1069G>A	NP_001073279.1:p.Ala357Thr
NM_001079811.2:c.1069G>A	NP_001073279.1:p.Ala357Thr
NM_001135602.1:c.766G>A	NP_001129074.1:p.Ala256Thr
NM_001135602.2:c.766G>A	NP_001129074.1:p.Ala256Thr
NM_001317040.1:c.1303G>A	NP_001303969.1:p.Ala435Thr
XR_001740634.1:n.1543-548C>T
NM_000404.4:c.1159G>A MANE Select	NP_000395.3:p.Ala387Thr
NM_001079811.3:c.1069G>A	NP_001073279.2:p.Ala357Thr
NM_001135602.3:c.766G>A	NP_001129074.2:p.Ala256Thr
NM_001317040.2:c.1303G>A	NP_001303969.2:p.Ala435Thr
NM_001393580.1:c.1159G>A	NP_001380509.1:p.Ala387Thr