Canonical Allele Identifier: CA2261612630

Gene: GFAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44913297T= , CM000679.2:g.44913297T=	GRCh38
NC_000017.10:g.42990665T= , CM000679.1:g.42990665T=	GRCh37
NC_000017.9:g.40346191T=	NCBI36
NG_008401.1:g.7250A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253408.11:c.752A=	ENSP00000253408.5:p.His251=
ENST00000435360.8:c.752A=	ENSP00000403962.1:p.His251=
ENST00000253408.10:c.752A=	ENSP00000253408.5:p.His251=
ENST00000435360.7:c.752A=	ENSP00000403962.1:p.His251=
ENST00000586127.6:n.1281A=
ENST00000586793.6:c.752A=	ENSP00000468500.2:p.His251=
ENST00000587997.6:n.228A=
ENST00000588735.3:c.752A= MANE Select	ENSP00000466598.2:p.His251=
ENST00000591327.2:n.1906A=
ENST00000592320.6:c.618+431A=	ENSP00000465320.1:n.618+431A=
ENST00000638281.1:c.752A=	ENSP00000491088.1:p.His251=
ENST00000638618.1:c.407A=	ENSP00000492832.1:p.His136=
ENST00000639277.1:c.752A=	ENSP00000492432.1:p.His251=
ENST00000640552.1:n.766A=
ENST00000253408.9:c.752A=	ENSP00000253408.4:p.His251=
ENST00000376990.8:c.*151A=	ENSP00000366189.4:n.*151A=
ENST00000435360.6:c.752A=	ENSP00000403962.1:p.His251=
ENST00000586793.5:c.752A=	ENSP00000468500.1:p.His251=
ENST00000587997.5:c.228A=
ENST00000588316.1:c.656A=	ENSP00000465629.1:p.His219=
ENST00000588735.1:c.82+2108A=	ENSP00000466598.1:n.82+2108A=
ENST00000588957.5:c.20A=	ENSP00000465565.1:p.His7=
ENST00000590922.1:n.402A=
ENST00000592320.5:c.618+431A=	ENSP00000465320.1:n.618+431A=
NM_001131019.2:c.752A=	NP_001124491.1:p.His251=
NM_001242376.1:c.752A=	NP_001229305.1:p.His251=
NM_002055.4:c.752A=	NP_002046.1:p.His251=
NM_001363846.1:c.752A=	NP_001350775.1:p.His251=
XM_024450690.1:c.956A=	XP_024306458.1:p.His319=
XM_024450691.1:c.956A=	XP_024306459.1:p.His319=
XM_024450692.1:c.956A=	XP_024306460.1:p.His319=
XM_024450693.1:c.956A=	XP_024306461.1:p.His319=
NM_002055.5:c.752A= MANE Select	NP_002046.1:p.His251=
NM_001131019.3:c.752A=	NP_001124491.1:p.His251=
NM_001242376.2:c.752A=	NP_001229305.1:p.His251=
NM_001242376.3:c.752A=	NP_001229305.1:p.His251=
NM_001363846.2:c.752A=	NP_001350775.1:p.His251=