Canonical Allele Identifier: CA2261610153

Gene: GFAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44907914A= , CM000679.2:g.44907914A=	GRCh38
NC_000017.10:g.42985282A= , CM000679.1:g.42985282A=	GRCh37
NC_000017.9:g.40340808A=	NCBI36
NG_008401.1:g.12633T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253408.11:c.1377+150T=	ENSP00000253408.5:n.1377+150T=
ENST00000253408.10:c.1377+150T=	ENSP00000253408.5:n.1377+150T=
ENST00000441312.2:n.110+150T=
ENST00000585543.6:n.410+150T=
ENST00000586125.2:c.342T=	ENSP00000467397.2:p.Thr114=
ENST00000588735.3:c.1257+150T= MANE Select	ENSP00000466598.2:n.1257+150T=
ENST00000589701.2:n.2164+150T=
ENST00000591880.2:c.506T=
ENST00000592065.2:n.625+150T=
ENST00000638304.1:c.176+150T=
ENST00000638400.1:c.92+150T=
ENST00000638488.1:n.721+150T=
ENST00000638618.1:c.912+150T=	ENSP00000492832.1:n.912+150T=
ENST00000638921.1:n.334T=
ENST00000639042.1:c.229+150T=
ENST00000639243.1:c.13+150T=
ENST00000639277.1:c.1257+150T=	ENSP00000492432.1:n.1257+150T=
ENST00000639369.1:c.107+150T=
ENST00000640545.1:c.63+150T=	ENSP00000491735.1:n.63+150T=
ENST00000640859.1:c.71+150T=
ENST00000253408.9:c.1257+150T=	ENSP00000253408.4:n.1257+150T=
ENST00000585543.5:n.410+150T=
ENST00000588735.1:c.135+150T=	ENSP00000466598.1:n.135+150T=
ENST00000589701.1:n.159+150T=
ENST00000591880.1:c.273T=	ENSP00000467530.1:p.Thr91=
ENST00000592065.1:n.51+150T=
ENST00000592706.5:n.129+150T=
NM_002055.4:c.1257+150T=	NP_002046.1:n.1257+150T=
NM_001363846.1:c.1377+150T=	NP_001350775.1:n.1377+150T=
XM_024450690.1:c.1581+150T=	XP_024306458.1:n.1581+150T=
XM_024450692.1:c.1461+150T=	XP_024306460.1:n.1461+150T=
NM_002055.5:c.1257+150T= MANE Select	NP_002046.1:n.1257+150T=
NM_001363846.2:c.1377+150T=	NP_001350775.1:n.1377+150T=