Canonical Allele Identifier: CA2840071791

Gene: GLB1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.33021672dup , CM000665.2:g.33021672dup	GRCh38
NC_000003.11:g.33063164dup , CM000665.1:g.33063164dup	GRCh37
NC_000003.10:g.33038168dup	NCBI36
NG_009005.1:g.80531dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307363.10:c.1144-17dup MANE Select	ENSP00000306920.4:n.1144-17dup
ENST00000307363.9:c.1144-17dup	ENSP00000306920.4:n.1144-17dup
ENST00000307377.12:c.751-17dup	ENSP00000305920.8:n.751-17dup
ENST00000399402.7:c.1054-17dup	ENSP00000382333.2:n.1054-17dup
ENST00000461475.5:n.243-17dup
ENST00000467571.5:n.181-17dup
ENST00000473477.1:n.176-17dup
ENST00000482097.5:n.519-17dup
ENST00000497796.5:n.396-17dup
NM_000404.2:c.1144-17dup	NP_000395.2:n.1144-17dup
NM_000404.3:c.1144-17dup	NP_000395.2:n.1144-17dup
NM_001079811.1:c.1054-17dup	NP_001073279.1:n.1054-17dup
NM_001079811.2:c.1054-17dup	NP_001073279.1:n.1054-17dup
NM_001135602.1:c.751-17dup	NP_001129074.1:n.751-17dup
NM_001135602.2:c.751-17dup	NP_001129074.1:n.751-17dup
NM_001317040.1:c.1288-17dup	NP_001303969.1:n.1288-17dup
XR_001740634.1:n.1543-516dup
NM_000404.4:c.1144-17dup MANE Select	NP_000395.3:n.1144-17dup
NM_001079811.3:c.1054-17dup	NP_001073279.2:n.1054-17dup
NM_001135602.3:c.751-17dup	NP_001129074.2:n.751-17dup
NM_001317040.2:c.1288-17dup	NP_001303969.2:n.1288-17dup
NM_001393580.1:c.1144-17dup	NP_001380509.1:n.1144-17dup