Canonical Allele Identifier: CA2261610212
Gene: GFAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44908049C= , CM000679.2:g.44908049C= GRCh38
NC_000017.10:g.42985417C= , CM000679.1:g.42985417C= GRCh37
NC_000017.9:g.40340943C= NCBI36
NG_008401.1:g.12498G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000253408.11:c.1377+15G= ENSP00000253408.5:n.1377+15G=
ENST00000253408.10:c.1377+15G= ENSP00000253408.5:n.1377+15G=
ENST00000441312.2:n.110+15G=
ENST00000585543.6:n.410+15G=
ENST00000586125.2:c.207G= ENSP00000467397.2:p.Leu69=
ENST00000588735.3:c.1257+15G= MANE Select ENSP00000466598.2:n.1257+15G=
ENST00000589701.2:n.2164+15G=
ENST00000591880.2:c.371G=
ENST00000592065.2:n.625+15G=
ENST00000638304.1:c.176+15G=
ENST00000638400.1:c.92+15G=
ENST00000638488.1:n.721+15G=
ENST00000638618.1:c.912+15G= ENSP00000492832.1:n.912+15G=
ENST00000638921.1:n.199G=
ENST00000639042.1:c.229+15G=
ENST00000639243.1:c.13+15G=
ENST00000639277.1:c.1257+15G= ENSP00000492432.1:n.1257+15G=
ENST00000639369.1:c.107+15G=
ENST00000640545.1:c.63+15G= ENSP00000491735.1:n.63+15G=
ENST00000640859.1:c.71+15G=
ENST00000253408.9:c.1257+15G= ENSP00000253408.4:n.1257+15G=
ENST00000585543.5:n.410+15G=
ENST00000588735.1:c.135+15G= ENSP00000466598.1:n.135+15G=
ENST00000589701.1:n.159+15G=
ENST00000591880.1:c.138G= ENSP00000467530.1:p.Leu46=
ENST00000592065.1:n.51+15G=
ENST00000592706.5:n.129+15G=
NM_002055.4:c.1257+15G= NP_002046.1:n.1257+15G=
NM_001363846.1:c.1377+15G= NP_001350775.1:n.1377+15G=
XM_024450690.1:c.1581+15G= XP_024306458.1:n.1581+15G=
XM_024450692.1:c.1461+15G= XP_024306460.1:n.1461+15G=
NM_002055.5:c.1257+15G= MANE Select NP_002046.1:n.1257+15G=
NM_001363846.2:c.1377+15G= NP_001350775.1:n.1377+15G=