Canonical Allele Identifier: CA2261612788

Gene: GFAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44913609_44913611delinsATC , CM000679.2:g.44913609_44913611delinsATC	GRCh38
NC_000017.10:g.42990977_42990979delinsATC , CM000679.1:g.42990977_42990979delinsATC	GRCh37
NC_000017.9:g.40346503_40346505delinsATC	NCBI36
NG_008401.1:g.6936_6938delinsGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253408.11:c.618+117_618+119delinsGAT	ENSP00000253408.5:n.618+117_618+119delinsGAT
ENST00000435360.8:c.618+117_618+119delinsGAT	ENSP00000403962.1:n.618+117_618+119delinsGAT
ENST00000253408.10:c.618+117_618+119delinsGAT	ENSP00000253408.5:n.618+117_618+119delinsGAT
ENST00000435360.7:c.618+117_618+119delinsGAT	ENSP00000403962.1:n.618+117_618+119delinsGAT
ENST00000586127.6:n.1147+117_1147+119delinsGAT
ENST00000586793.6:c.618+117_618+119delinsGAT	ENSP00000468500.2:n.618+117_618+119delinsGAT
ENST00000587997.6:n.86_88delinsGAT
ENST00000588735.3:c.618+117_618+119delinsGAT MANE Select	ENSP00000466598.2:n.618+117_618+119delinsGAT
ENST00000591327.2:n.1772+117_1772+119delinsGAT
ENST00000592320.6:c.618+117_618+119delinsGAT	ENSP00000465320.1:n.618+117_618+119delinsGAT
ENST00000638281.1:c.618+117_618+119delinsGAT	ENSP00000491088.1:n.618+117_618+119delinsGAT
ENST00000638618.1:c.273+117_273+119delinsGAT	ENSP00000492832.1:n.273+117_273+119delinsGAT
ENST00000639277.1:c.618+117_618+119delinsGAT	ENSP00000492432.1:n.618+117_618+119delinsGAT
ENST00000640552.1:n.632+117_632+119delinsGAT
ENST00000253408.9:c.618+117_618+119delinsGAT	ENSP00000253408.4:n.618+117_618+119delinsGAT
ENST00000376990.8:c.*17+117_*17+119delinsGAT	ENSP00000366189.4:n.*17+117_*17+119delinsGAT
ENST00000435360.6:c.618+117_618+119delinsGAT	ENSP00000403962.1:n.618+117_618+119delinsGAT
ENST00000585728.5:c.*262+117_*262+119delinsGAT	ENSP00000465208.1:n.*262+117_*262+119delinsGAT
ENST00000586127.5:c.-44+117_-44+119delinsGAT	ENSP00000464795.1:n.-44+117_-44+119delinsGAT
ENST00000586793.5:c.618+117_618+119delinsGAT	ENSP00000468500.1:n.618+117_618+119delinsGAT
ENST00000587997.5:c.86_88delinsGAT
ENST00000588316.1:c.523-181_523-179delinsGAT	ENSP00000465629.1:n.523-181_523-179delinsGAT
ENST00000588735.1:c.82+1794_82+1796delinsGAT	ENSP00000466598.1:n.82+1794_82+1796delinsGAT
ENST00000588957.5:c.-115+117_-115+119delinsGAT	ENSP00000465565.1:n.-115+117_-115+119delinsGAT
ENST00000590922.1:n.88_90delinsGAT
ENST00000591327.1:n.571+117_571+119delinsGAT
ENST00000592320.5:c.618+117_618+119delinsGAT	ENSP00000465320.1:n.618+117_618+119delinsGAT
NM_001131019.2:c.618+117_618+119delinsGAT	NP_001124491.1:n.618+117_618+119delinsGAT
NM_001242376.1:c.618+117_618+119delinsGAT	NP_001229305.1:n.618+117_618+119delinsGAT
NM_002055.4:c.618+117_618+119delinsGAT	NP_002046.1:n.618+117_618+119delinsGAT
NM_001363846.1:c.618+117_618+119delinsGAT	NP_001350775.1:n.618+117_618+119delinsGAT
XM_024450690.1:c.822+117_822+119delinsGAT	XP_024306458.1:n.822+117_822+119delinsGAT
XM_024450691.1:c.822+117_822+119delinsGAT	XP_024306459.1:n.822+117_822+119delinsGAT
XM_024450692.1:c.822+117_822+119delinsGAT	XP_024306460.1:n.822+117_822+119delinsGAT
XM_024450693.1:c.822+117_822+119delinsGAT	XP_024306461.1:n.822+117_822+119delinsGAT
NM_002055.5:c.618+117_618+119delinsGAT MANE Select	NP_002046.1:n.618+117_618+119delinsGAT
NM_001131019.3:c.618+117_618+119delinsGAT	NP_001124491.1:n.618+117_618+119delinsGAT
NM_001242376.2:c.618+117_618+119delinsGAT	NP_001229305.1:n.618+117_618+119delinsGAT
NM_001242376.3:c.618+117_618+119delinsGAT	NP_001229305.1:n.618+117_618+119delinsGAT
NM_001363846.2:c.618+117_618+119delinsGAT	NP_001350775.1:n.618+117_618+119delinsGAT