Canonical Allele Identifier: CA2261611685

Gene: GFAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44911357_44911358delinsGC , CM000679.2:g.44911357_44911358delinsGC	GRCh38
NC_000017.10:g.42988725_42988726delinsGC , CM000679.1:g.42988725_42988726delinsGC	GRCh37
NC_000017.9:g.40344251_40344252delinsGC	NCBI36
NG_008401.1:g.9189_9190delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253408.11:c.1005_1006delinsGC	ENSP00000253408.5:p.Gly335=
ENST00000435360.8:c.1005_1006delinsGC	ENSP00000403962.1:p.Gly335=
ENST00000253408.10:c.1005_1006delinsGC	ENSP00000253408.5:p.Gly335=
ENST00000435360.7:c.1005_1006delinsGC	ENSP00000403962.1:p.Gly335=
ENST00000585543.6:n.158_159delinsGC
ENST00000586127.6:n.1534_1535delinsGC
ENST00000586793.6:c.907-37_907-36delinsGC	ENSP00000468500.2:n.907-37_907-36delinsGC
ENST00000587997.6:n.481_482delinsGC
ENST00000588735.3:c.1005_1006delinsGC MANE Select	ENSP00000466598.2:p.Gly335=
ENST00000591327.2:n.2159_2160delinsGC
ENST00000592320.6:c.619-37_619-36delinsGC	ENSP00000465320.1:n.619-37_619-36delinsGC
ENST00000638281.1:c.1005_1006delinsGC	ENSP00000491088.1:p.Gly335=
ENST00000638618.1:c.660_661delinsGC	ENSP00000492832.1:p.Gly220=
ENST00000639277.1:c.1005_1006delinsGC	ENSP00000492432.1:p.Gly335=
ENST00000640552.1:n.1019_1020delinsGC
ENST00000253408.9:c.1005_1006delinsGC	ENSP00000253408.4:p.Gly335=
ENST00000376990.8:c.*404_*405delinsGC	ENSP00000366189.4:n.*404_*405delinsGC
ENST00000435360.6:c.1005_1006delinsGC	ENSP00000403962.1:p.Gly335=
ENST00000585543.5:n.158_159delinsGC
ENST00000586793.5:c.1005_1006delinsGC	ENSP00000468500.1:p.Gly335=
ENST00000587997.5:c.481_482delinsGC
ENST00000588640.5:n.385_386delinsGC
ENST00000588735.1:c.83-3242_83-3241delinsGC	ENSP00000466598.1:n.83-3242_83-3241delinsGC
ENST00000592320.5:c.619-37_619-36delinsGC	ENSP00000465320.1:n.619-37_619-36delinsGC
NM_001131019.2:c.1005_1006delinsGC	NP_001124491.1:p.Gly335=
NM_001242376.1:c.1005_1006delinsGC	NP_001229305.1:p.Gly335=
NM_002055.4:c.1005_1006delinsGC	NP_002046.1:p.Gly335=
NM_001363846.1:c.1005_1006delinsGC	NP_001350775.1:p.Gly335=
XM_024450690.1:c.1209_1210delinsGC	XP_024306458.1:p.Gly403=
XM_024450691.1:c.1209_1210delinsGC	XP_024306459.1:p.Gly403=
XM_024450692.1:c.1209_1210delinsGC	XP_024306460.1:p.Gly403=
XM_024450693.1:c.1209_1210delinsGC	XP_024306461.1:p.Gly403=
NM_002055.5:c.1005_1006delinsGC MANE Select	NP_002046.1:p.Gly335=
NM_001131019.3:c.1005_1006delinsGC	NP_001124491.1:p.Gly335=
NM_001242376.2:c.1005_1006delinsGC	NP_001229305.1:p.Gly335=
NM_001242376.3:c.1005_1006delinsGC	NP_001229305.1:p.Gly335=
NM_001363846.2:c.1005_1006delinsGC	NP_001350775.1:p.Gly335=