Canonical Allele Identifier: CA2261612658
Gene: GFAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44913353G= , CM000679.2:g.44913353G= GRCh38
NC_000017.10:g.42990721G= , CM000679.1:g.42990721G= GRCh37
NC_000017.9:g.40346247G= NCBI36
NG_008401.1:g.7194C=

Transcript Alleles

HGVS Amino-acid change
ENST00000253408.11:c.696C= ENSP00000253408.5:p.Thr232=
ENST00000435360.8:c.696C= ENSP00000403962.1:p.Thr232=
ENST00000253408.10:c.696C= ENSP00000253408.5:p.Thr232=
ENST00000435360.7:c.696C= ENSP00000403962.1:p.Thr232=
ENST00000586127.6:n.1225C=
ENST00000586793.6:c.696C= ENSP00000468500.2:p.Thr232=
ENST00000587997.6:n.172C=
ENST00000588735.3:c.696C= MANE Select ENSP00000466598.2:p.Thr232=
ENST00000591327.2:n.1850C=
ENST00000592320.6:c.618+375C= ENSP00000465320.1:n.618+375C=
ENST00000638281.1:c.696C= ENSP00000491088.1:p.Thr232=
ENST00000638618.1:c.351C= ENSP00000492832.1:p.Thr117=
ENST00000639277.1:c.696C= ENSP00000492432.1:p.Thr232=
ENST00000640552.1:n.710C=
ENST00000253408.9:c.696C= ENSP00000253408.4:p.Thr232=
ENST00000376990.8:c.*95C= ENSP00000366189.4:n.*95C=
ENST00000435360.6:c.696C= ENSP00000403962.1:p.Thr232=
ENST00000585728.5:c.*340C= ENSP00000465208.1:n.*340C=
ENST00000586127.5:c.35C= ENSP00000464795.1:p.Pro12=
ENST00000586793.5:c.696C= ENSP00000468500.1:p.Thr232=
ENST00000587997.5:c.172C=
ENST00000588316.1:c.600C= ENSP00000465629.1:p.Thr200=
ENST00000588735.1:c.82+2052C= ENSP00000466598.1:n.82+2052C=
ENST00000588957.5:c.-37C= ENSP00000465565.1:n.-37C=
ENST00000590922.1:n.346C=
ENST00000592320.5:c.618+375C= ENSP00000465320.1:n.618+375C=
NM_001131019.2:c.696C= NP_001124491.1:p.Thr232=
NM_001242376.1:c.696C= NP_001229305.1:p.Thr232=
NM_002055.4:c.696C= NP_002046.1:p.Thr232=
NM_001363846.1:c.696C= NP_001350775.1:p.Thr232=
XM_024450690.1:c.900C= XP_024306458.1:p.Thr300=
XM_024450691.1:c.900C= XP_024306459.1:p.Thr300=
XM_024450692.1:c.900C= XP_024306460.1:p.Thr300=
XM_024450693.1:c.900C= XP_024306461.1:p.Thr300=
NM_002055.5:c.696C= MANE Select NP_002046.1:p.Thr232=
NM_001131019.3:c.696C= NP_001124491.1:p.Thr232=
NM_001242376.2:c.696C= NP_001229305.1:p.Thr232=
NM_001242376.3:c.696C= NP_001229305.1:p.Thr232=
NM_001363846.2:c.696C= NP_001350775.1:p.Thr232=