Canonical Allele Identifier: CA2261613614

Gene: GFAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44915251_44915252delinsCG , CM000679.2:g.44915251_44915252delinsCG	GRCh38
NC_000017.10:g.42992619_42992620delinsCG , CM000679.1:g.42992619_42992620delinsCG	GRCh37
NC_000017.9:g.40348145_40348146delinsCG	NCBI36
NG_008401.1:g.5295_5296delinsCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000253408.11:c.235_236delinsCG	ENSP00000253408.5:p.Arg79=
ENST00000435360.8:c.235_236delinsCG	ENSP00000403962.1:p.Arg79=
ENST00000253408.10:c.235_236delinsCG	ENSP00000253408.5:p.Arg79=
ENST00000435360.7:c.235_236delinsCG	ENSP00000403962.1:p.Arg79=
ENST00000586793.6:c.235_236delinsCG	ENSP00000468500.2:p.Arg79=
ENST00000588735.3:c.235_236delinsCG MANE Select	ENSP00000466598.2:p.Arg79=
ENST00000591327.2:n.248_249delinsCG
ENST00000592320.6:c.235_236delinsCG	ENSP00000465320.1:p.Arg79=
ENST00000638281.1:c.235_236delinsCG	ENSP00000491088.1:p.Arg79=
ENST00000639277.1:c.235_236delinsCG	ENSP00000492432.1:p.Arg79=
ENST00000640552.1:n.249_250delinsCG
ENST00000253408.9:c.235_236delinsCG	ENSP00000253408.4:p.Arg79=
ENST00000376990.8:c.235_236delinsCG	ENSP00000366189.4:p.Arg79=
ENST00000435360.6:c.235_236delinsCG	ENSP00000403962.1:p.Arg79=
ENST00000585728.5:c.181+54_181+55delinsCG	ENSP00000465208.1:n.181+54_181+55delinsCG...
ENST00000586793.5:c.235_236delinsCG	ENSP00000468500.1:p.Arg79=
ENST00000588037.1:c.235_236delinsCG	ENSP00000466163.1:p.Arg79=
ENST00000588316.1:c.235_236delinsCG	ENSP00000465629.1:p.Arg79=
ENST00000588735.1:c.82+153_82+154delinsCG	ENSP00000466598.1:n.82+153_82+154delinsCG...
ENST00000588957.5:c.-272+565_-272+566delinsCG	ENSP00000465565.1:n.-272+565_-272+566deli...
ENST00000591327.1:n.249_250delinsCG
ENST00000592320.5:c.235_236delinsCG	ENSP00000465320.1:p.Arg79=
NM_001131019.2:c.235_236delinsCG	NP_001124491.1:p.Arg79=
NM_001242376.1:c.235_236delinsCG	NP_001229305.1:p.Arg79=
NM_002055.4:c.235_236delinsCG	NP_002046.1:p.Arg79=
NM_001363846.1:c.235_236delinsCG	NP_001350775.1:p.Arg79=
XM_024450690.1:c.235_236delinsCG	XP_024306458.1:p.Arg79=
XM_024450691.1:c.235_236delinsCG	XP_024306459.1:p.Arg79=
XM_024450692.1:c.235_236delinsCG	XP_024306460.1:p.Arg79=
XM_024450693.1:c.235_236delinsCG	XP_024306461.1:p.Arg79=
NM_002055.5:c.235_236delinsCG MANE Select	NP_002046.1:p.Arg79=
NM_001131019.3:c.235_236delinsCG	NP_001124491.1:p.Arg79=
NM_001242376.2:c.235_236delinsCG	NP_001229305.1:p.Arg79=
NM_001242376.3:c.235_236delinsCG	NP_001229305.1:p.Arg79=
NM_001363846.2:c.235_236delinsCG	NP_001350775.1:p.Arg79=