Canonical Allele Identifier: CA2577539529

Gene: GLB1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.33018406C>A , CM000665.2:g.33018406C>A	GRCh38
NC_000003.11:g.33059898C>A , CM000665.1:g.33059898C>A	GRCh37
NC_000003.10:g.33034902C>A	NCBI36
NG_009005.1:g.83797G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307363.10:c.1347+42G>T MANE Select	ENSP00000306920.4:n.1347+42G>T
ENST00000307363.9:c.1347+42G>T	ENSP00000306920.4:n.1347+42G>T
ENST00000307377.12:c.954+42G>T	ENSP00000305920.8:n.954+42G>T
ENST00000399402.7:c.1257+42G>T	ENSP00000382333.2:n.1257+42G>T
ENST00000461475.5:n.446+42G>T
ENST00000467571.5:n.384+42G>T
ENST00000497796.5:n.599+42G>T
NM_000404.2:c.1347+42G>T	NP_000395.2:n.1347+42G>T
NM_000404.3:c.1347+42G>T	NP_000395.2:n.1347+42G>T
NM_001079811.1:c.1257+42G>T	NP_001073279.1:n.1257+42G>T
NM_001079811.2:c.1257+42G>T	NP_001073279.1:n.1257+42G>T
NM_001135602.1:c.954+42G>T	NP_001129074.1:n.954+42G>T
NM_001135602.2:c.954+42G>T	NP_001129074.1:n.954+42G>T
NM_001317040.1:c.1491+42G>T	NP_001303969.1:n.1491+42G>T
NM_000404.4:c.1347+42G>T MANE Select	NP_000395.3:n.1347+42G>T
NM_001079811.3:c.1257+42G>T	NP_001073279.2:n.1257+42G>T
NM_001135602.3:c.954+42G>T	NP_001129074.2:n.954+42G>T
NM_001317040.2:c.1491+42G>T	NP_001303969.2:n.1491+42G>T
NM_001393580.1:c.1347+42G>T	NP_001380509.1:n.1347+42G>T