Canonical Allele Identifier: CA2261610232

Gene: GFAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44908094C= , CM000679.2:g.44908094C=	GRCh38
NC_000017.10:g.42985462C= , CM000679.1:g.42985462C=	GRCh37
NC_000017.9:g.40340988C=	NCBI36
NG_008401.1:g.12453G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253408.11:c.1347G=	ENSP00000253408.5:p.Val449=
ENST00000253408.10:c.1347G=	ENSP00000253408.5:p.Val449=
ENST00000441312.2:n.80G=
ENST00000585543.6:n.380G=
ENST00000586125.2:c.162G=	ENSP00000467397.2:p.Val54=
ENST00000588735.3:c.1227G= MANE Select	ENSP00000466598.2:p.Val409=
ENST00000589701.2:n.2134G=
ENST00000591880.2:c.326G=
ENST00000592065.2:n.595G=
ENST00000638304.1:c.146G=
ENST00000638400.1:c.62G=
ENST00000638488.1:n.691G=
ENST00000638618.1:c.882G=	ENSP00000492832.1:p.Val294=
ENST00000638921.1:n.154G=
ENST00000639042.1:c.199G=
ENST00000639277.1:c.1227G=	ENSP00000492432.1:p.Val409=
ENST00000639369.1:c.77G=
ENST00000640545.1:c.33G=	ENSP00000491735.1:p.Val11=
ENST00000640859.1:c.41G=
ENST00000253408.9:c.1227G=	ENSP00000253408.4:p.Val409=
ENST00000585543.5:n.380G=
ENST00000588735.1:c.105G=	ENSP00000466598.1:p.Val35=
ENST00000589701.1:n.129G=
ENST00000591880.1:c.93G=	ENSP00000467530.1:p.Val31=
ENST00000592065.1:n.21G=
ENST00000592706.5:n.99G=
NM_002055.4:c.1227G=	NP_002046.1:p.Val409=
NM_001363846.1:c.1347G=	NP_001350775.1:p.Val449=
XM_024450690.1:c.1551G=	XP_024306458.1:p.Val517=
XM_024450692.1:c.1431G=	XP_024306460.1:p.Val477=
NM_002055.5:c.1227G= MANE Select	NP_002046.1:p.Val409=
NM_001363846.2:c.1347G=	NP_001350775.1:p.Val449=