Canonical Allele Identifier: CA2839257097
Gene: GFAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44915156_44915157del , CM000679.2:g.44915156_44915157del GRCh38
NC_000017.10:g.42992524_42992525del , CM000679.1:g.42992524_42992525del GRCh37
NC_000017.9:g.40348050_40348051del NCBI36
NG_008401.1:g.5390_5391del

Transcript Alleles

HGVS Amino-acid Change
ENST00000253408.11:c.330_331del ENSP00000253408.5:p.Lys111AlafsTer8
ENST00000435360.8:c.330_331del ENSP00000403962.1:p.Lys111AlafsTer8
ENST00000253408.10:c.330_331del ENSP00000253408.5:p.Lys111AlafsTer8
ENST00000435360.7:c.330_331del ENSP00000403962.1:p.Lys111AlafsTer8
ENST00000586793.6:c.330_331del ENSP00000468500.2:p.Lys111AlafsTer8
ENST00000588735.3:c.330_331del MANE Select ENSP00000466598.2:p.Lys111AlafsTer8
ENST00000591327.2:n.343_344del
ENST00000592320.6:c.330_331del ENSP00000465320.1:p.Lys111AlafsTer8
ENST00000638281.1:c.330_331del ENSP00000491088.1:p.Lys111AlafsTer8
ENST00000639277.1:c.330_331del ENSP00000492432.1:p.Lys111AlafsTer8
ENST00000640552.1:n.344_345del
ENST00000253408.9:c.330_331del ENSP00000253408.4:p.Lys111AlafsTer8
ENST00000376990.8:c.330_331del ENSP00000366189.4:p.Lys111AlafsTer8
ENST00000435360.6:c.330_331del ENSP00000403962.1:p.Lys111AlafsTer8
ENST00000585728.5:c.182-22_182-21del ENSP00000465208.1:n.182-22_182-21del
ENST00000586793.5:c.330_331del ENSP00000468500.1:p.Lys111AlafsTer8
ENST00000588037.1:c.330_331del ENSP00000466163.1:p.Lys111AlafsTer8
ENST00000588316.1:c.330_331del ENSP00000465629.1:p.Lys111AlafsTer8
ENST00000588735.1:c.82+248_82+249del ENSP00000466598.1:n.82+248_82+249del
ENST00000588957.5:c.-272+660_-272+661del ENSP00000465565.1:n.-272+660_-272+661del
ENST00000591327.1:n.344_345del
ENST00000592320.5:c.330_331del ENSP00000465320.1:p.Lys111AlafsTer8
NM_001131019.2:c.330_331del NP_001124491.1:p.Lys111AlafsTer8
NM_001242376.1:c.330_331del NP_001229305.1:p.Lys111AlafsTer8
NM_002055.4:c.330_331del NP_002046.1:p.Lys111AlafsTer8
NM_001363846.1:c.330_331del NP_001350775.1:p.Lys111AlafsTer8
XM_024450690.1:c.330_331del XP_024306458.1:p.Lys111AlafsTer8
XM_024450691.1:c.330_331del XP_024306459.1:p.Lys111AlafsTer8
XM_024450692.1:c.330_331del XP_024306460.1:p.Lys111AlafsTer8
XM_024450693.1:c.330_331del XP_024306461.1:p.Lys111AlafsTer8
NM_002055.5:c.330_331del MANE Select NP_002046.1:p.Lys111AlafsTer8
NM_001131019.3:c.330_331del NP_001124491.1:p.Lys111AlafsTer8
NM_001242376.2:c.330_331del NP_001229305.1:p.Lys111AlafsTer8
NM_001242376.3:c.330_331del NP_001229305.1:p.Lys111AlafsTer8
NM_001363846.2:c.330_331del NP_001350775.1:p.Lys111AlafsTer8