Canonical Allele Identifier: CA1355987561
Gene: GLB1 HGNC NCBI

Linked Data

dbSNP Id: rs1697492280

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.33021696dup , CM000665.2:g.33021696dup GRCh38
NC_000003.11:g.33063188dup , CM000665.1:g.33063188dup GRCh37
NC_000003.10:g.33038192dup NCBI36
NG_009005.1:g.80507dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000307363.10:c.1144-41dup MANE Select ENSP00000306920.4:n.1144-41dup
ENST00000307363.9:c.1144-41dup ENSP00000306920.4:n.1144-41dup
ENST00000307377.12:c.751-41dup ENSP00000305920.8:n.751-41dup
ENST00000399402.7:c.1054-41dup ENSP00000382333.2:n.1054-41dup
ENST00000461475.5:n.243-41dup
ENST00000467571.5:n.181-41dup
ENST00000473477.1:n.176-41dup
ENST00000482097.5:n.519-41dup
ENST00000497796.5:n.396-41dup
NM_000404.2:c.1144-41dup NP_000395.2:n.1144-41dup
NM_000404.3:c.1144-41dup NP_000395.2:n.1144-41dup
NM_001079811.1:c.1054-41dup NP_001073279.1:n.1054-41dup
NM_001079811.2:c.1054-41dup NP_001073279.1:n.1054-41dup
NM_001135602.1:c.751-41dup NP_001129074.1:n.751-41dup
NM_001135602.2:c.751-41dup NP_001129074.1:n.751-41dup
NM_001317040.1:c.1288-41dup NP_001303969.1:n.1288-41dup
XR_001740634.1:n.1543-492dup
NM_000404.4:c.1144-41dup MANE Select NP_000395.3:n.1144-41dup
NM_001079811.3:c.1054-41dup NP_001073279.2:n.1054-41dup
NM_001135602.3:c.751-41dup NP_001129074.2:n.751-41dup
NM_001317040.2:c.1288-41dup NP_001303969.2:n.1288-41dup
NM_001393580.1:c.1144-41dup NP_001380509.1:n.1144-41dup