Canonical Allele Identifier: CA2261613481
Gene: GFAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44914999G= , CM000679.2:g.44914999G= GRCh38
NC_000017.10:g.42992367G= , CM000679.1:g.42992367G= GRCh37
NC_000017.9:g.40347893G= NCBI36
NG_008401.1:g.5548C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000253408.11:c.461+27C= ENSP00000253408.5:n.461+27C=
ENST00000435360.8:c.461+27C= ENSP00000403962.1:n.461+27C=
ENST00000253408.10:c.461+27C= ENSP00000253408.5:n.461+27C=
ENST00000435360.7:c.461+27C= ENSP00000403962.1:n.461+27C=
ENST00000586127.6:n.80C=
ENST00000586793.6:c.461+27C= ENSP00000468500.2:n.461+27C=
ENST00000588735.3:c.461+27C= MANE Select ENSP00000466598.2:n.461+27C=
ENST00000591327.2:n.501C=
ENST00000592320.6:c.461+27C= ENSP00000465320.1:n.461+27C=
ENST00000638281.1:c.461+27C= ENSP00000491088.1:n.461+27C=
ENST00000638618.1:c.116+27C= ENSP00000492832.1:n.116+27C=
ENST00000639277.1:c.461+27C= ENSP00000492432.1:n.461+27C=
ENST00000640552.1:n.475+27C=
ENST00000253408.9:c.461+27C= ENSP00000253408.4:n.461+27C=
ENST00000376990.8:c.461+27C= ENSP00000366189.4:n.461+27C=
ENST00000435360.6:c.461+27C= ENSP00000403962.1:n.461+27C=
ENST00000585728.5:c.*105+27C= ENSP00000465208.1:n.*105+27C=
ENST00000586793.5:c.461+27C= ENSP00000468500.1:n.461+27C=
ENST00000588037.1:c.461+27C= ENSP00000466163.1:n.461+27C=
ENST00000588316.1:c.461+27C= ENSP00000465629.1:n.461+27C=
ENST00000588735.1:c.82+406C= ENSP00000466598.1:n.82+406C=
ENST00000588957.5:c.-272+818C= ENSP00000465565.1:n.-272+818C=
ENST00000591327.1:n.475+27C=
ENST00000592320.5:c.461+27C= ENSP00000465320.1:n.461+27C=
NM_001131019.2:c.461+27C= NP_001124491.1:n.461+27C=
NM_001242376.1:c.461+27C= NP_001229305.1:n.461+27C=
NM_002055.4:c.461+27C= NP_002046.1:n.461+27C=
NM_001363846.1:c.461+27C= NP_001350775.1:n.461+27C=
XM_024450690.1:c.461+27C= XP_024306458.1:n.461+27C=
XM_024450691.1:c.461+27C= XP_024306459.1:n.461+27C=
XM_024450692.1:c.461+27C= XP_024306460.1:n.461+27C=
XM_024450693.1:c.461+27C= XP_024306461.1:n.461+27C=
NM_002055.5:c.461+27C= MANE Select NP_002046.1:n.461+27C=
NM_001131019.3:c.461+27C= NP_001124491.1:n.461+27C=
NM_001242376.2:c.461+27C= NP_001229305.1:n.461+27C=
NM_001242376.3:c.461+27C= NP_001229305.1:n.461+27C=
NM_001363846.2:c.461+27C= NP_001350775.1:n.461+27C=