Canonical Allele Identifier: CA2261610145

Gene: GFAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44907887A= , CM000679.2:g.44907887A=	GRCh38
NC_000017.10:g.42985255A= , CM000679.1:g.42985255A=	GRCh37
NC_000017.9:g.40340781A=	NCBI36
NG_008401.1:g.12660T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253408.11:c.1377+177T=	ENSP00000253408.5:n.1377+177T=
ENST00000253408.10:c.1377+177T=	ENSP00000253408.5:n.1377+177T=
ENST00000441312.2:n.110+177T=
ENST00000585543.6:n.410+177T=
ENST00000586125.2:c.369T=	ENSP00000467397.2:p.Pro123=
ENST00000588735.3:c.1257+177T= MANE Select	ENSP00000466598.2:n.1257+177T=
ENST00000589701.2:n.2164+177T=
ENST00000591880.2:c.533T=
ENST00000592065.2:n.625+177T=
ENST00000638304.1:c.176+177T=
ENST00000638400.1:c.92+177T=
ENST00000638488.1:n.721+177T=
ENST00000638618.1:c.912+177T=	ENSP00000492832.1:n.912+177T=
ENST00000638921.1:n.361T=
ENST00000639042.1:c.229+177T=
ENST00000639243.1:c.13+177T=
ENST00000639277.1:c.1257+177T=	ENSP00000492432.1:n.1257+177T=
ENST00000639369.1:c.107+177T=
ENST00000640545.1:c.63+177T=	ENSP00000491735.1:n.63+177T=
ENST00000640859.1:c.71+177T=
ENST00000253408.9:c.1257+177T=	ENSP00000253408.4:n.1257+177T=
ENST00000585543.5:n.410+177T=
ENST00000588735.1:c.135+177T=	ENSP00000466598.1:n.135+177T=
ENST00000589701.1:n.159+177T=
ENST00000591880.1:c.300T=	ENSP00000467530.1:p.Pro100=
ENST00000592065.1:n.51+177T=
ENST00000592706.5:n.129+177T=
NM_002055.4:c.1257+177T=	NP_002046.1:n.1257+177T=
NM_001363846.1:c.1377+177T=	NP_001350775.1:n.1377+177T=
XM_024450690.1:c.1581+177T=	XP_024306458.1:n.1581+177T=
XM_024450692.1:c.1461+177T=	XP_024306460.1:n.1461+177T=
NM_002055.5:c.1257+177T= MANE Select	NP_002046.1:n.1257+177T=
NM_001363846.2:c.1377+177T=	NP_001350775.1:n.1377+177T=