Canonical Allele Identifier: CA2261609936

Gene: GFAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44907369T= , CM000679.2:g.44907369T=	GRCh38
NC_000017.10:g.42984737T= , CM000679.1:g.42984737T=	GRCh37
NC_000017.9:g.40340263T=	NCBI36
NG_008401.1:g.13178A=

Transcript Alleles

HGVS	Amino-acid Change
NM_002055.5:c.1277A= MANE Select	NP_002046.1:p.Gln426=
ENST00000588735.3:c.1277A= MANE Select	ENSP00000466598.2:p.Gln426=
NM_001363846.1:c.1397A=	NP_001350775.1:p.Gln466=
NM_001363846.2:c.1397A=	NP_001350775.1:p.Gln466=
NM_002055.4:c.1277A=	NP_002046.1:p.Gln426=
ENST00000253408.10:c.1397A=	ENSP00000253408.5:p.Gln466=
ENST00000253408.11:c.1397A=	ENSP00000253408.5:p.Gln466=
ENST00000253408.9:c.1277A=	ENSP00000253408.4:p.Gln426=
ENST00000441312.2:n.110+695A=
ENST00000585543.5:n.430A=
ENST00000585543.6:n.430A=
ENST00000586125.2:c.887A=	ENSP00000467397.2:n.887A=
ENST00000588735.1:c.155A=	ENSP00000466598.1:p.Gln52=
ENST00000589701.1:n.179A=
ENST00000589701.2:n.2184A=
ENST00000591880.2:c.1051A=
ENST00000592065.1:n.51+695A=
ENST00000592065.2:n.625+695A=
ENST00000592706.5:n.149A=
ENST00000638304.1:c.176+695A=
ENST00000638400.1:c.92+695A=
ENST00000638488.1:n.721+695A=
ENST00000638618.1:c.912+695A=	ENSP00000492832.1:n.912+695A=
ENST00000638921.1:n.879A=
ENST00000639042.1:c.229+695A=
ENST00000639243.1:c.13+695A=
ENST00000639277.1:c.1257+695A=	ENSP00000492432.1:n.1257+695A=
ENST00000639369.1:c.107+695A=
ENST00000640545.1:c.63+695A=	ENSP00000491735.1:n.63+695A=
ENST00000640859.1:c.71+695A=
XM_024450690.1:c.1601A=	XP_024306458.1:p.Gln534=
XM_024450692.1:c.1481A=	XP_024306460.1:p.Gln494=