Canonical Allele Identifier: CA2261610220

Gene: GFAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44908066C= , CM000679.2:g.44908066C=	GRCh38
NC_000017.10:g.42985434C= , CM000679.1:g.42985434C=	GRCh37
NC_000017.9:g.40340960C=	NCBI36
NG_008401.1:g.12481G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253408.11:c.1375G=	ENSP00000253408.5:p.Glu459=
ENST00000253408.10:c.1375G=	ENSP00000253408.5:p.Glu459=
ENST00000441312.2:n.108G=
ENST00000585543.6:n.408G=
ENST00000586125.2:c.190G=	ENSP00000467397.2:p.Glu64=
ENST00000588735.3:c.1255G= MANE Select	ENSP00000466598.2:p.Glu419=
ENST00000589701.2:n.2162G=
ENST00000591880.2:c.354G=
ENST00000592065.2:n.623G=
ENST00000638304.1:c.174G=
ENST00000638400.1:c.90G=
ENST00000638488.1:n.719G=
ENST00000638618.1:c.910G=	ENSP00000492832.1:p.Glu304=
ENST00000638921.1:n.182G=
ENST00000639042.1:c.227G=
ENST00000639243.1:c.11G=
ENST00000639277.1:c.1255G=	ENSP00000492432.1:p.Glu419=
ENST00000639369.1:c.105G=
ENST00000640545.1:c.61G=	ENSP00000491735.1:p.Glu21=
ENST00000640859.1:c.69G=
ENST00000253408.9:c.1255G=	ENSP00000253408.4:p.Glu419=
ENST00000585543.5:n.408G=
ENST00000588735.1:c.133G=	ENSP00000466598.1:p.Glu45=
ENST00000589701.1:n.157G=
ENST00000591880.1:c.121G=	ENSP00000467530.1:p.Glu41=
ENST00000592065.1:n.49G=
ENST00000592706.5:n.127G=
NM_002055.4:c.1255G=	NP_002046.1:p.Glu419=
NM_001363846.1:c.1375G=	NP_001350775.1:p.Glu459=
XM_024450690.1:c.1579G=	XP_024306458.1:p.Glu527=
XM_024450692.1:c.1459G=	XP_024306460.1:p.Glu487=
NM_002055.5:c.1255G= MANE Select	NP_002046.1:p.Glu419=
NM_001363846.2:c.1375G=	NP_001350775.1:p.Glu459=