Canonical Allele Identifier: CA2261613712

Gene: GFAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44915438_44915439delinsAG , CM000679.2:g.44915438_44915439delinsAG	GRCh38
NC_000017.10:g.42992806_42992807delinsAG , CM000679.1:g.42992806_42992807delinsAG	GRCh37
NC_000017.9:g.40348332_40348333delinsAG	NCBI36
NG_008401.1:g.5108_5109delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253408.11:c.48_49delinsCT	ENSP00000253408.5:p.Ser16=
ENST00000435360.8:c.48_49delinsCT	ENSP00000403962.1:p.Ser16=
ENST00000253408.10:c.48_49delinsCT	ENSP00000253408.5:p.Ser16=
ENST00000435360.7:c.48_49delinsCT	ENSP00000403962.1:p.Ser16=
ENST00000586793.6:c.48_49delinsCT	ENSP00000468500.2:p.Ser16=
ENST00000588735.3:c.48_49delinsCT MANE Select	ENSP00000466598.2:p.Ser16=
ENST00000591327.2:n.61_62delinsCT
ENST00000592320.6:c.48_49delinsCT	ENSP00000465320.1:p.Ser16=
ENST00000638281.1:c.48_49delinsCT	ENSP00000491088.1:p.Ser16=
ENST00000639277.1:c.48_49delinsCT	ENSP00000492432.1:p.Ser16=
ENST00000640552.1:n.62_63delinsCT
ENST00000253408.9:c.48_49delinsCT	ENSP00000253408.4:p.Ser16=
ENST00000376990.8:c.48_49delinsCT	ENSP00000366189.4:p.Ser16=
ENST00000435360.6:c.48_49delinsCT	ENSP00000403962.1:p.Ser16=
ENST00000585728.5:c.48_49delinsCT	ENSP00000465208.1:p.Ser16=
ENST00000586793.5:c.48_49delinsCT	ENSP00000468500.1:p.Ser16=
ENST00000588037.1:c.48_49delinsCT	ENSP00000466163.1:p.Ser16=
ENST00000588316.1:c.48_49delinsCT	ENSP00000465629.1:p.Ser16=
ENST00000588735.1:c.48_49delinsCT	ENSP00000466598.1:p.Ser16=
ENST00000588957.5:c.-272+378_-272+379delinsCT	ENSP00000465565.1:n.-272+378_-272+379delinsCT
ENST00000591327.1:n.62_63delinsCT
ENST00000592320.5:c.48_49delinsCT	ENSP00000465320.1:p.Ser16=
NM_001131019.2:c.48_49delinsCT	NP_001124491.1:p.Ser16=
NM_001242376.1:c.48_49delinsCT	NP_001229305.1:p.Ser16=
NM_002055.4:c.48_49delinsCT	NP_002046.1:p.Ser16=
NM_001363846.1:c.48_49delinsCT	NP_001350775.1:p.Ser16=
XM_024450690.1:c.48_49delinsCT	XP_024306458.1:p.Ser16=
XM_024450691.1:c.48_49delinsCT	XP_024306459.1:p.Ser16=
XM_024450692.1:c.48_49delinsCT	XP_024306460.1:p.Ser16=
XM_024450693.1:c.48_49delinsCT	XP_024306461.1:p.Ser16=
NM_002055.5:c.48_49delinsCT MANE Select	NP_002046.1:p.Ser16=
NM_001131019.3:c.48_49delinsCT	NP_001124491.1:p.Ser16=
NM_001242376.2:c.48_49delinsCT	NP_001229305.1:p.Ser16=
NM_001242376.3:c.48_49delinsCT	NP_001229305.1:p.Ser16=
NM_001363846.2:c.48_49delinsCT	NP_001350775.1:p.Ser16=