Canonical Allele Identifier: CA2261610143

Gene: GFAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44907885G= , CM000679.2:g.44907885G=	GRCh38
NC_000017.10:g.42985253G= , CM000679.1:g.42985253G=	GRCh37
NC_000017.9:g.40340779G=	NCBI36
NG_008401.1:g.12662C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253408.11:c.1377+179C=	ENSP00000253408.5:n.1377+179C=
ENST00000253408.10:c.1377+179C=	ENSP00000253408.5:n.1377+179C=
ENST00000441312.2:n.110+179C=
ENST00000585543.6:n.410+179C=
ENST00000586125.2:c.371C=	ENSP00000467397.2:p.Pro124=
ENST00000588735.3:c.1257+179C= MANE Select	ENSP00000466598.2:n.1257+179C=
ENST00000589701.2:n.2164+179C=
ENST00000591880.2:c.535C=
ENST00000592065.2:n.625+179C=
ENST00000638304.1:c.176+179C=
ENST00000638400.1:c.92+179C=
ENST00000638488.1:n.721+179C=
ENST00000638618.1:c.912+179C=	ENSP00000492832.1:n.912+179C=
ENST00000638921.1:n.363C=
ENST00000639042.1:c.229+179C=
ENST00000639243.1:c.13+179C=
ENST00000639277.1:c.1257+179C=	ENSP00000492432.1:n.1257+179C=
ENST00000639369.1:c.107+179C=
ENST00000640545.1:c.63+179C=	ENSP00000491735.1:n.63+179C=
ENST00000640859.1:c.71+179C=
ENST00000253408.9:c.1257+179C=	ENSP00000253408.4:n.1257+179C=
ENST00000585543.5:n.410+179C=
ENST00000588735.1:c.135+179C=	ENSP00000466598.1:n.135+179C=
ENST00000589701.1:n.159+179C=
ENST00000591880.1:c.302C=	ENSP00000467530.1:p.Pro101=
ENST00000592065.1:n.51+179C=
ENST00000592706.5:n.129+179C=
NM_002055.4:c.1257+179C=	NP_002046.1:n.1257+179C=
NM_001363846.1:c.1377+179C=	NP_001350775.1:n.1377+179C=
XM_024450690.1:c.1581+179C=	XP_024306458.1:n.1581+179C=
XM_024450692.1:c.1461+179C=	XP_024306460.1:n.1461+179C=
NM_002055.5:c.1257+179C= MANE Select	NP_002046.1:n.1257+179C=
NM_001363846.2:c.1377+179C=	NP_001350775.1:n.1377+179C=