Canonical Allele Identifier: CA2261613746

Gene: GFAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44915492T= , CM000679.2:g.44915492T=	GRCh38
NC_000017.10:g.42992860T= , CM000679.1:g.42992860T=	GRCh37
NC_000017.9:g.40348386T=	NCBI36
NG_008401.1:g.5055A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253408.11:c.-6A=	ENSP00000253408.5:n.-6A=
ENST00000435360.8:c.-6A=	ENSP00000403962.1:n.-6A=
ENST00000253408.10:c.-6A=	ENSP00000253408.5:n.-6A=
ENST00000435360.7:c.-6A=	ENSP00000403962.1:n.-6A=
ENST00000586793.6:c.-6A=	ENSP00000468500.2:n.-6A=
ENST00000588735.3:c.-6A= MANE Select	ENSP00000466598.2:n.-6A=
ENST00000591327.2:n.8A=
ENST00000592320.6:c.-6A=	ENSP00000465320.1:n.-6A=
ENST00000639277.1:c.-6A=	ENSP00000492432.1:n.-6A=
ENST00000640552.1:n.9A=
ENST00000253408.9:c.-6A=	ENSP00000253408.4:n.-6A=
ENST00000376990.8:c.-6A=	ENSP00000366189.4:n.-6A=
ENST00000435360.6:c.-6A=	ENSP00000403962.1:n.-6A=
ENST00000585728.5:c.-6A=	ENSP00000465208.1:n.-6A=
ENST00000586793.5:c.-6A=	ENSP00000468500.1:n.-6A=
ENST00000588037.1:c.-6A=	ENSP00000466163.1:n.-6A=
ENST00000588735.1:c.-6A=	ENSP00000466598.1:n.-6A=
ENST00000588957.5:c.-272+325A=	ENSP00000465565.1:n.-272+325A=
ENST00000591327.1:n.9A=
ENST00000592320.5:c.-6A=	ENSP00000465320.1:n.-6A=
ENST00000593179.1:c.-6A=	ENSP00000467106.1:n.-6A=
NM_001131019.2:c.-6A=	NP_001124491.1:n.-6A=
NM_001242376.1:c.-6A=	NP_001229305.1:n.-6A=
NM_002055.4:c.-6A=	NP_002046.1:n.-6A=
NM_001363846.1:c.-6A=	NP_001350775.1:n.-6A=
XM_024450690.1:c.-6A=	XP_024306458.1:n.-6A=
XM_024450691.1:c.-6A=	XP_024306459.1:n.-6A=
XM_024450692.1:c.-6A=	XP_024306460.1:n.-6A=
XM_024450693.1:c.-6A=	XP_024306461.1:n.-6A=
NM_002055.5:c.-6A= MANE Select	NP_002046.1:n.-6A=
NM_001131019.3:c.-6A=	NP_001124491.1:n.-6A=
NM_001242376.2:c.-6A=	NP_001229305.1:n.-6A=
NM_001242376.3:c.-6A=	NP_001229305.1:n.-6A=
NM_001363846.2:c.-6A=	NP_001350775.1:n.-6A=