Canonical Allele Identifier: CA2261610175

Gene: GFAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44907971T= , CM000679.2:g.44907971T=	GRCh38
NC_000017.10:g.42985339T= , CM000679.1:g.42985339T=	GRCh37
NC_000017.9:g.40340865T=	NCBI36
NG_008401.1:g.12576A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253408.11:c.1377+93A=	ENSP00000253408.5:n.1377+93A=
ENST00000253408.10:c.1377+93A=	ENSP00000253408.5:n.1377+93A=
ENST00000441312.2:n.110+93A=
ENST00000585543.6:n.410+93A=
ENST00000586125.2:c.285A=	ENSP00000467397.2:p.Glu95=
ENST00000588735.3:c.1257+93A= MANE Select	ENSP00000466598.2:n.1257+93A=
ENST00000589701.2:n.2164+93A=
ENST00000591880.2:c.449A=
ENST00000592065.2:n.625+93A=
ENST00000638304.1:c.176+93A=
ENST00000638400.1:c.92+93A=
ENST00000638488.1:n.721+93A=
ENST00000638618.1:c.912+93A=	ENSP00000492832.1:n.912+93A=
ENST00000638921.1:n.277A=
ENST00000639042.1:c.229+93A=
ENST00000639243.1:c.13+93A=
ENST00000639277.1:c.1257+93A=	ENSP00000492432.1:n.1257+93A=
ENST00000639369.1:c.107+93A=
ENST00000640545.1:c.63+93A=	ENSP00000491735.1:n.63+93A=
ENST00000640859.1:c.71+93A=
ENST00000253408.9:c.1257+93A=	ENSP00000253408.4:n.1257+93A=
ENST00000585543.5:n.410+93A=
ENST00000588735.1:c.135+93A=	ENSP00000466598.1:n.135+93A=
ENST00000589701.1:n.159+93A=
ENST00000591880.1:c.216A=	ENSP00000467530.1:p.Glu72=
ENST00000592065.1:n.51+93A=
ENST00000592706.5:n.129+93A=
NM_002055.4:c.1257+93A=	NP_002046.1:n.1257+93A=
NM_001363846.1:c.1377+93A=	NP_001350775.1:n.1377+93A=
XM_024450690.1:c.1581+93A=	XP_024306458.1:n.1581+93A=
XM_024450692.1:c.1461+93A=	XP_024306460.1:n.1461+93A=
NM_002055.5:c.1257+93A= MANE Select	NP_002046.1:n.1257+93A=
NM_001363846.2:c.1377+93A=	NP_001350775.1:n.1377+93A=