Canonical Allele Identifier: CA2261610221

Gene: GFAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44908071T= , CM000679.2:g.44908071T=	GRCh38
NC_000017.10:g.42985439T= , CM000679.1:g.42985439T=	GRCh37
NC_000017.9:g.40340965T=	NCBI36
NG_008401.1:g.12476A=

Transcript Alleles

HGVS	Amino-acid Change
NM_002055.5:c.1250A= MANE Select	NP_002046.1:p.Asp417=
ENST00000588735.3:c.1250A= MANE Select	ENSP00000466598.2:p.Asp417=
NM_001363846.1:c.1370A=	NP_001350775.1:p.Asp457=
NM_001363846.2:c.1370A=	NP_001350775.1:p.Asp457=
NM_002055.4:c.1250A=	NP_002046.1:p.Asp417=
ENST00000253408.10:c.1370A=	ENSP00000253408.5:p.Asp457=
ENST00000253408.11:c.1370A=	ENSP00000253408.5:p.Asp457=
ENST00000253408.9:c.1250A=	ENSP00000253408.4:p.Asp417=
ENST00000441312.2:n.103A=
ENST00000585543.5:n.403A=
ENST00000585543.6:n.403A=
ENST00000586125.2:c.185A=	ENSP00000467397.2:p.Asp62=
ENST00000588735.1:c.128A=	ENSP00000466598.1:p.Asp43=
ENST00000589701.1:n.152A=
ENST00000589701.2:n.2157A=
ENST00000591880.1:c.116A=	ENSP00000467530.1:p.Asp39=
ENST00000591880.2:c.349A=
ENST00000592065.1:n.44A=
ENST00000592065.2:n.618A=
ENST00000592706.5:n.122A=
ENST00000638304.1:c.169A=
ENST00000638400.1:c.85A=
ENST00000638488.1:n.714A=
ENST00000638618.1:c.905A=	ENSP00000492832.1:p.Asp302=
ENST00000638921.1:n.177A=
ENST00000639042.1:c.222A=
ENST00000639243.1:c.6A=
ENST00000639277.1:c.1250A=	ENSP00000492432.1:p.Asp417=
ENST00000639369.1:c.100A=
ENST00000640545.1:c.56A=	ENSP00000491735.1:p.Asp19=
ENST00000640859.1:c.64A=
XM_024450690.1:c.1574A=	XP_024306458.1:p.Asp525=
XM_024450692.1:c.1454A=	XP_024306460.1:p.Asp485=