Canonical Allele Identifier: CA432957641

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.33097014_33097024del , CM000665.2:g.33097014_33097024del GRCh38
NC_000003.11:g.33138506_33138516del , CM000665.1:g.33138506_33138516del GRCh37
NC_000003.10:g.33113510_33113520del NCBI36
NG_009005.1:g.5183_5193del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307363.10:c.66_75+1del (GLB1)
ENST00000342462.5:c.-410_-400del (TMPPE) MANE Select ENSP00000343398.4:n.-410_-400del
ENST00000307363.9:c.66_75+1del (GLB1)
ENST00000307377.12:c.66_75+1del (GLB1)
ENST00000415454.1:c.66_75+1del (GLB1)
ENST00000436768.1:c.66_75+1del (GLB1)
ENST00000438227.1:c.66_75+1del (GLB1)
ENST00000440656.1:c.-158_-149+1del (GLB1)
ENST00000464355.1:n.24_33+1del (GLB1)
ENST00000482097.5:n.99_108+1del (GLB1)
ENST00000485698.5:n.127_136+1del (GLB1)
ENST00000498537.5:n.123_132+1del (GLB1)
NM_000404.2:c.66_75+1del (GLB1)
NM_000404.3:c.66_75+1del (GLB1)
NM_001135602.1:c.66_75+1del (GLB1)
NM_001135602.2:c.66_75+1del (GLB1)
NM_001317040.1:c.66_75+1del (GLB1)
NM_000404.4:c.66_75+1del (GLB1)
NM_001039770.3:c.-410_-400del (TMPPE) MANE Select NP_001034859.2:n.-410_-400del
NM_001136238.2:c.-306_-296del (TMPPE) NP_001129710.1:n.-306_-296del
NM_001135602.3:c.66_75+1del (GLB1)
NM_001317040.2:c.66_75+1del (GLB1)
NM_001393580.1:c.66_75+1del (GLB1)