Canonical Allele Identifier: CA2576294505
Gene: GFAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44913328_44913337del , CM000679.2:g.44913328_44913337del GRCh38
NC_000017.10:g.42990696_42990705del , CM000679.1:g.42990696_42990705del GRCh37
NC_000017.9:g.40346222_40346231del NCBI36
NG_008401.1:g.7211_7220del

Transcript Alleles

HGVS Amino-acid Change
ENST00000253408.11:c.713_722del ENSP00000253408.5:p.Ile238SerfsTer24
ENST00000435360.8:c.713_722del ENSP00000403962.1:p.Ile238SerfsTer24
ENST00000253408.10:c.713_722del ENSP00000253408.5:p.Ile238SerfsTer24
ENST00000435360.7:c.713_722del ENSP00000403962.1:p.Ile238SerfsTer24
ENST00000586127.6:n.1242_1251del
ENST00000586793.6:c.713_722del ENSP00000468500.2:p.Ile238SerfsTer24
ENST00000587997.6:n.189_198del
ENST00000588735.3:c.713_722del MANE Select ENSP00000466598.2:p.Ile238SerfsTer24
ENST00000591327.2:n.1867_1876del
ENST00000592320.6:c.618+392_618+401del ENSP00000465320.1:n.618+392_618+401del
ENST00000638281.1:c.713_722del ENSP00000491088.1:p.Ile238SerfsTer24
ENST00000638618.1:c.368_377del ENSP00000492832.1:p.Ile123SerfsTer24
ENST00000639277.1:c.713_722del ENSP00000492432.1:p.Ile238SerfsTer24
ENST00000640552.1:n.727_736del
ENST00000253408.9:c.713_722del ENSP00000253408.4:p.Ile238SerfsTer24
ENST00000376990.8:c.*112_*121del ENSP00000366189.4:n.*112_*121del
ENST00000435360.6:c.713_722del ENSP00000403962.1:p.Ile238SerfsTer24
ENST00000585728.5:c.*357_*366del ENSP00000465208.1:n.*357_*366del
ENST00000586793.5:c.713_722del ENSP00000468500.1:p.Ile238SerfsTer24
ENST00000587997.5:c.189_198del
ENST00000588316.1:c.617_626del ENSP00000465629.1:p.Ile206SerfsTer24
ENST00000588735.1:c.82+2069_82+2078del ENSP00000466598.1:n.82+2069_82+2078del
ENST00000588957.5:c.-20_-11del ENSP00000465565.1:n.-20_-11del
ENST00000590922.1:n.363_372del
ENST00000592320.5:c.618+392_618+401del ENSP00000465320.1:n.618+392_618+401del
NM_001131019.2:c.713_722del NP_001124491.1:p.Ile238SerfsTer24
NM_001242376.1:c.713_722del NP_001229305.1:p.Ile238SerfsTer24
NM_002055.4:c.713_722del NP_002046.1:p.Ile238SerfsTer24
NM_001363846.1:c.713_722del NP_001350775.1:p.Ile238SerfsTer24
XM_024450690.1:c.917_926del XP_024306458.1:p.Ile306SerfsTer24
XM_024450691.1:c.917_926del XP_024306459.1:p.Ile306SerfsTer24
XM_024450692.1:c.917_926del XP_024306460.1:p.Ile306SerfsTer24
XM_024450693.1:c.917_926del XP_024306461.1:p.Ile306SerfsTer24
NM_002055.5:c.713_722del MANE Select NP_002046.1:p.Ile238SerfsTer24
NM_001131019.3:c.713_722del NP_001124491.1:p.Ile238SerfsTer24
NM_001242376.2:c.713_722del NP_001229305.1:p.Ile238SerfsTer24
NM_001242376.3:c.713_722del NP_001229305.1:p.Ile238SerfsTer24
NM_001363846.2:c.713_722del NP_001350775.1:p.Ile238SerfsTer24