Canonical Allele Identifier: CA2261613577
Gene: GFAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44915180G= , CM000679.2:g.44915180G= GRCh38
NC_000017.10:g.42992548G= , CM000679.1:g.42992548G= GRCh37
NC_000017.9:g.40348074G= NCBI36
NG_008401.1:g.5367C=

Transcript Alleles

HGVS Amino-acid change
ENST00000253408.11:c.307C= ENSP00000253408.5:p.Gln103=
ENST00000435360.8:c.307C= ENSP00000403962.1:p.Gln103=
ENST00000253408.10:c.307C= ENSP00000253408.5:p.Gln103=
ENST00000435360.7:c.307C= ENSP00000403962.1:p.Gln103=
ENST00000586793.6:c.307C= ENSP00000468500.2:p.Gln103=
ENST00000588735.3:c.307C= MANE Select ENSP00000466598.2:p.Gln103=
ENST00000591327.2:n.320C=
ENST00000592320.6:c.307C= ENSP00000465320.1:p.Gln103=
ENST00000638281.1:c.307C= ENSP00000491088.1:p.Gln103=
ENST00000639277.1:c.307C= ENSP00000492432.1:p.Gln103=
ENST00000640552.1:n.321C=
ENST00000253408.9:c.307C= ENSP00000253408.4:p.Gln103=
ENST00000376990.8:c.307C= ENSP00000366189.4:p.Gln103=
ENST00000435360.6:c.307C= ENSP00000403962.1:p.Gln103=
ENST00000585728.5:c.182-45C= ENSP00000465208.1:n.182-45C=
ENST00000586793.5:c.307C= ENSP00000468500.1:p.Gln103=
ENST00000588037.1:c.307C= ENSP00000466163.1:p.Gln103=
ENST00000588316.1:c.307C= ENSP00000465629.1:p.Gln103=
ENST00000588735.1:c.82+225C= ENSP00000466598.1:n.82+225C=
ENST00000588957.5:c.-272+637C= ENSP00000465565.1:n.-272+637C=
ENST00000591327.1:n.321C=
ENST00000592320.5:c.307C= ENSP00000465320.1:p.Gln103=
NM_001131019.2:c.307C= NP_001124491.1:p.Gln103=
NM_001242376.1:c.307C= NP_001229305.1:p.Gln103=
NM_002055.4:c.307C= NP_002046.1:p.Gln103=
NM_001363846.1:c.307C= NP_001350775.1:p.Gln103=
XM_024450690.1:c.307C= XP_024306458.1:p.Gln103=
XM_024450691.1:c.307C= XP_024306459.1:p.Gln103=
XM_024450692.1:c.307C= XP_024306460.1:p.Gln103=
XM_024450693.1:c.307C= XP_024306461.1:p.Gln103=
NM_002055.5:c.307C= MANE Select NP_002046.1:p.Gln103=
NM_001131019.3:c.307C= NP_001124491.1:p.Gln103=
NM_001242376.2:c.307C= NP_001229305.1:p.Gln103=
NM_001242376.3:c.307C= NP_001229305.1:p.Gln103=
NM_001363846.2:c.307C= NP_001350775.1:p.Gln103=