Canonical Allele Identifier: CA2261610225

Gene: GFAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44908074C= , CM000679.2:g.44908074C=	GRCh38
NC_000017.10:g.42985442C= , CM000679.1:g.42985442C=	GRCh37
NC_000017.9:g.40340968C=	NCBI36
NG_008401.1:g.12473G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253408.11:c.1367G=	ENSP00000253408.5:p.Arg456=
ENST00000253408.10:c.1367G=	ENSP00000253408.5:p.Arg456=
ENST00000441312.2:n.100G=
ENST00000585543.6:n.400G=
ENST00000586125.2:c.182G=	ENSP00000467397.2:p.Arg61=
ENST00000588735.3:c.1247G= MANE Select	ENSP00000466598.2:p.Arg416=
ENST00000589701.2:n.2154G=
ENST00000591880.2:c.346G=
ENST00000592065.2:n.615G=
ENST00000638304.1:c.166G=
ENST00000638400.1:c.82G=
ENST00000638488.1:n.711G=
ENST00000638618.1:c.902G=	ENSP00000492832.1:p.Arg301=
ENST00000638921.1:n.174G=
ENST00000639042.1:c.219G=
ENST00000639243.1:c.3G=
ENST00000639277.1:c.1247G=	ENSP00000492432.1:p.Arg416=
ENST00000639369.1:c.97G=
ENST00000640545.1:c.53G=	ENSP00000491735.1:p.Arg18=
ENST00000640859.1:c.61G=
ENST00000253408.9:c.1247G=	ENSP00000253408.4:p.Arg416=
ENST00000585543.5:n.400G=
ENST00000588735.1:c.125G=	ENSP00000466598.1:p.Arg42=
ENST00000589701.1:n.149G=
ENST00000591880.1:c.113G=	ENSP00000467530.1:p.Arg38=
ENST00000592065.1:n.41G=
ENST00000592706.5:n.119G=
NM_002055.4:c.1247G=	NP_002046.1:p.Arg416=
NM_001363846.1:c.1367G=	NP_001350775.1:p.Arg456=
XM_024450690.1:c.1571G=	XP_024306458.1:p.Arg524=
XM_024450692.1:c.1451G=	XP_024306460.1:p.Arg484=
NM_002055.5:c.1247G= MANE Select	NP_002046.1:p.Arg416=
NM_001363846.2:c.1367G=	NP_001350775.1:p.Arg456=