Canonical Allele Identifier: CA1356021479

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.33097136G= , CM000665.2:g.33097136G= GRCh38
NC_000003.11:g.33138628G= , CM000665.1:g.33138628G= GRCh37
NC_000003.10:g.33113632G= NCBI36
NG_009005.1:g.5067C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307363.10:c.-51C= (GLB1) MANE Select ENSP00000306920.4:n.-51C=
ENST00000342462.5:c.-526C= (TMPPE) MANE Select ENSP00000343398.4:n.-526C=
ENST00000307363.9:c.-51C= (GLB1) ENSP00000306920.4:n.-51C=
ENST00000307377.12:c.-51C= (GLB1) ENSP00000305920.8:n.-51C=
ENST00000436768.1:c.-51C= (GLB1) ENSP00000387989.1:n.-51C=
ENST00000438227.1:c.-51C= (GLB1) ENSP00000401250.1:n.-51C=
ENST00000440656.1:c.-274C= (GLB1) ENSP00000411769.1:n.-274C=
ENST00000485698.5:n.11C= (GLB1)
ENST00000498537.5:n.7C= (GLB1)
NM_000404.2:c.-51C= (GLB1) NP_000395.2:n.-51C=
NM_000404.3:c.-51C= (GLB1) NP_000395.2:n.-51C=
NM_001135602.1:c.-51C= (GLB1) NP_001129074.1:n.-51C=
NM_001135602.2:c.-51C= (GLB1) NP_001129074.1:n.-51C=
NM_001317040.1:c.-51C= (GLB1) NP_001303969.1:n.-51C=
NM_000404.4:c.-51C= (GLB1) MANE Select NP_000395.3:n.-51C=
NM_001039770.3:c.-526C= (TMPPE) MANE Select NP_001034859.2:n.-526C=
NM_001136238.2:c.-422C= (TMPPE) NP_001129710.1:n.-422C=
NM_001135602.3:c.-51C= (GLB1) NP_001129074.2:n.-51C=
NM_001317040.2:c.-51C= (GLB1) NP_001303969.2:n.-51C=
NM_001393580.1:c.-51C= (GLB1) NP_001380509.1:n.-51C=