Canonical Allele Identifier: CA1356021388

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.33096997T= , CM000665.2:g.33096997T= GRCh38
NC_000003.11:g.33138489T= , CM000665.1:g.33138489T= GRCh37
NC_000003.10:g.33113493T= NCBI36
NG_009005.1:g.5206A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307363.10:c.75+14A= (GLB1) MANE Select ENSP00000306920.4:n.75+14A=
ENST00000342462.5:c.-387A= (TMPPE) MANE Select ENSP00000343398.4:n.-387A=
ENST00000307363.9:c.75+14A= (GLB1) ENSP00000306920.4:n.75+14A=
ENST00000307377.12:c.75+14A= (GLB1) ENSP00000305920.8:n.75+14A=
ENST00000415454.1:c.75+14A= (GLB1) ENSP00000411813.1:n.75+14A=
ENST00000436768.1:c.75+14A= (GLB1) ENSP00000387989.1:n.75+14A=
ENST00000438227.1:c.75+14A= (GLB1) ENSP00000401250.1:n.75+14A=
ENST00000440656.1:c.-149+14A= (GLB1) ENSP00000411769.1:n.-149+14A=
ENST00000464355.1:n.33+14A= (GLB1)
ENST00000482097.5:n.108+14A= (GLB1)
ENST00000485698.5:n.136+14A= (GLB1)
ENST00000498537.5:n.132+14A= (GLB1)
NM_000404.2:c.75+14A= (GLB1) NP_000395.2:n.75+14A=
NM_000404.3:c.75+14A= (GLB1) NP_000395.2:n.75+14A=
NM_001135602.1:c.75+14A= (GLB1) NP_001129074.1:n.75+14A=
NM_001135602.2:c.75+14A= (GLB1) NP_001129074.1:n.75+14A=
NM_001317040.1:c.75+14A= (GLB1) NP_001303969.1:n.75+14A=
NM_000404.4:c.75+14A= (GLB1) MANE Select NP_000395.3:n.75+14A=
NM_001039770.3:c.-387A= (TMPPE) MANE Select NP_001034859.2:n.-387A=
NM_001136238.2:c.-283A= (TMPPE) NP_001129710.1:n.-283A=
NM_001135602.3:c.75+14A= (GLB1) NP_001129074.2:n.75+14A=
NM_001317040.2:c.75+14A= (GLB1) NP_001303969.2:n.75+14A=
NM_001393580.1:c.75+14A= (GLB1) NP_001380509.1:n.75+14A=