Canonical Allele Identifier: CA2261612733

Gene: GFAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44913507C= , CM000679.2:g.44913507C=	GRCh38
NC_000017.10:g.42990875C= , CM000679.1:g.42990875C=	GRCh37
NC_000017.9:g.40346401C=	NCBI36
NG_008401.1:g.7040G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253408.11:c.619-77G=	ENSP00000253408.5:n.619-77G=
ENST00000435360.8:c.619-77G=	ENSP00000403962.1:n.619-77G=
ENST00000253408.10:c.619-77G=	ENSP00000253408.5:n.619-77G=
ENST00000435360.7:c.619-77G=	ENSP00000403962.1:n.619-77G=
ENST00000586127.6:n.1148-77G=
ENST00000586793.6:c.619-77G=	ENSP00000468500.2:n.619-77G=
ENST00000587997.6:n.95-77G=
ENST00000588735.3:c.619-77G= MANE Select	ENSP00000466598.2:n.619-77G=
ENST00000591327.2:n.1773-77G=
ENST00000592320.6:c.618+221G=	ENSP00000465320.1:n.618+221G=
ENST00000638281.1:c.619-77G=	ENSP00000491088.1:n.619-77G=
ENST00000638618.1:c.274-77G=	ENSP00000492832.1:n.274-77G=
ENST00000639277.1:c.619-77G=	ENSP00000492432.1:n.619-77G=
ENST00000640552.1:n.633-77G=
ENST00000253408.9:c.619-77G=	ENSP00000253408.4:n.619-77G=
ENST00000376990.8:c.*18-77G=	ENSP00000366189.4:n.*18-77G=
ENST00000435360.6:c.619-77G=	ENSP00000403962.1:n.619-77G=
ENST00000585728.5:c.*263-77G=	ENSP00000465208.1:n.*263-77G=
ENST00000586127.5:c.-43-77G=	ENSP00000464795.1:n.-43-77G=
ENST00000586793.5:c.619-77G=	ENSP00000468500.1:n.619-77G=
ENST00000587997.5:c.95-77G=
ENST00000588316.1:c.523-77G=	ENSP00000465629.1:n.523-77G=
ENST00000588735.1:c.82+1898G=	ENSP00000466598.1:n.82+1898G=
ENST00000588957.5:c.-114-77G=	ENSP00000465565.1:n.-114-77G=
ENST00000590922.1:n.192G=
ENST00000591327.1:n.572-77G=
ENST00000592320.5:c.618+221G=	ENSP00000465320.1:n.618+221G=
NM_001131019.2:c.619-77G=	NP_001124491.1:n.619-77G=
NM_001242376.1:c.619-77G=	NP_001229305.1:n.619-77G=
NM_002055.4:c.619-77G=	NP_002046.1:n.619-77G=
NM_001363846.1:c.619-77G=	NP_001350775.1:n.619-77G=
XM_024450690.1:c.823-77G=	XP_024306458.1:n.823-77G=
XM_024450691.1:c.823-77G=	XP_024306459.1:n.823-77G=
XM_024450692.1:c.823-77G=	XP_024306460.1:n.823-77G=
XM_024450693.1:c.823-77G=	XP_024306461.1:n.823-77G=
NM_002055.5:c.619-77G= MANE Select	NP_002046.1:n.619-77G=
NM_001131019.3:c.619-77G=	NP_001124491.1:n.619-77G=
NM_001242376.2:c.619-77G=	NP_001229305.1:n.619-77G=
NM_001242376.3:c.619-77G=	NP_001229305.1:n.619-77G=
NM_001363846.2:c.619-77G=	NP_001350775.1:n.619-77G=