Canonical Allele Identifier: CA2261610112

Gene: GFAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44907818A= , CM000679.2:g.44907818A=	GRCh38
NC_000017.10:g.42985186A= , CM000679.1:g.42985186A=	GRCh37
NC_000017.9:g.40340712A=	NCBI36
NG_008401.1:g.12729T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253408.11:c.1377+246T=	ENSP00000253408.5:n.1377+246T=
ENST00000253408.10:c.1377+246T=	ENSP00000253408.5:n.1377+246T=
ENST00000441312.2:n.110+246T=
ENST00000585543.6:n.410+246T=
ENST00000586125.2:c.438T=	ENSP00000467397.2:n.438T=
ENST00000588735.3:c.1257+246T= MANE Select	ENSP00000466598.2:n.1257+246T=
ENST00000589701.2:n.2164+246T=
ENST00000591880.2:c.602T=
ENST00000592065.2:n.625+246T=
ENST00000638304.1:c.176+246T=
ENST00000638400.1:c.92+246T=
ENST00000638488.1:n.721+246T=
ENST00000638618.1:c.912+246T=	ENSP00000492832.1:n.912+246T=
ENST00000638921.1:n.430T=
ENST00000639042.1:c.229+246T=
ENST00000639243.1:c.13+246T=
ENST00000639277.1:c.1257+246T=	ENSP00000492432.1:n.1257+246T=
ENST00000639369.1:c.107+246T=
ENST00000640545.1:c.63+246T=	ENSP00000491735.1:n.63+246T=
ENST00000640859.1:c.71+246T=
ENST00000253408.9:c.1257+246T=	ENSP00000253408.4:n.1257+246T=
ENST00000585543.5:n.410+246T=
ENST00000588735.1:c.135+246T=	ENSP00000466598.1:n.135+246T=
ENST00000589701.1:n.159+246T=
ENST00000591880.1:c.369T=	ENSP00000467530.1:n.369T=
ENST00000592065.1:n.51+246T=
ENST00000592706.5:n.129+246T=
NM_002055.4:c.1257+246T=	NP_002046.1:n.1257+246T=
NM_001363846.1:c.1377+246T=	NP_001350775.1:n.1377+246T=
XM_024450690.1:c.1581+246T=	XP_024306458.1:n.1581+246T=
XM_024450692.1:c.1461+246T=	XP_024306460.1:n.1461+246T=
NM_002055.5:c.1257+246T= MANE Select	NP_002046.1:n.1257+246T=
NM_001363846.2:c.1377+246T=	NP_001350775.1:n.1377+246T=