Canonical Allele Identifier: CA2261611699

Gene: GFAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44911382C= , CM000679.2:g.44911382C=	GRCh38
NC_000017.10:g.42988750C= , CM000679.1:g.42988750C=	GRCh37
NC_000017.9:g.40344276C=	NCBI36
NG_008401.1:g.9165G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000253408.11:c.981G=	ENSP00000253408.5:p.Ala327=
ENST00000435360.8:c.981G=	ENSP00000403962.1:p.Ala327=
ENST00000253408.10:c.981G=	ENSP00000253408.5:p.Ala327=
ENST00000435360.7:c.981G=	ENSP00000403962.1:p.Ala327=
ENST00000585543.6:n.134G=
ENST00000586127.6:n.1510G=
ENST00000586793.6:c.907-61G=	ENSP00000468500.2:n.907-61G=
ENST00000587997.6:n.457G=
ENST00000588735.3:c.981G= MANE Select	ENSP00000466598.2:p.Ala327=
ENST00000591327.2:n.2135G=
ENST00000592320.6:c.619-61G=	ENSP00000465320.1:n.619-61G=
ENST00000638281.1:c.981G=	ENSP00000491088.1:p.Ala327=
ENST00000638618.1:c.636G=	ENSP00000492832.1:p.Ala212=
ENST00000639277.1:c.981G=	ENSP00000492432.1:p.Ala327=
ENST00000640552.1:n.995G=
ENST00000253408.9:c.981G=	ENSP00000253408.4:p.Ala327=
ENST00000376990.8:c.*380G=	ENSP00000366189.4:n.*380G=
ENST00000435360.6:c.981G=	ENSP00000403962.1:p.Ala327=
ENST00000585543.5:n.134G=
ENST00000586793.5:c.981G=	ENSP00000468500.1:p.Ala327=
ENST00000587997.5:c.457G=
ENST00000588640.5:n.361G=
ENST00000588735.1:c.83-3266G=	ENSP00000466598.1:n.83-3266G=
ENST00000592320.5:c.619-61G=	ENSP00000465320.1:n.619-61G=
NM_001131019.2:c.981G=	NP_001124491.1:p.Ala327=
NM_001242376.1:c.981G=	NP_001229305.1:p.Ala327=
NM_002055.4:c.981G=	NP_002046.1:p.Ala327=
NM_001363846.1:c.981G=	NP_001350775.1:p.Ala327=
XM_024450690.1:c.1185G=	XP_024306458.1:p.Ala395=
XM_024450691.1:c.1185G=	XP_024306459.1:p.Ala395=
XM_024450692.1:c.1185G=	XP_024306460.1:p.Ala395=
XM_024450693.1:c.1185G=	XP_024306461.1:p.Ala395=
NM_002055.5:c.981G= MANE Select	NP_002046.1:p.Ala327=
NM_001131019.3:c.981G=	NP_001124491.1:p.Ala327=
NM_001242376.2:c.981G=	NP_001229305.1:p.Ala327=
NM_001242376.3:c.981G=	NP_001229305.1:p.Ala327=
NM_001363846.2:c.981G=	NP_001350775.1:p.Ala327=