Canonical Allele Identifier: CA2261610252

Gene: GFAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44908133G= , CM000679.2:g.44908133G=	GRCh38
NC_000017.10:g.42985501G= , CM000679.1:g.42985501G=	GRCh37
NC_000017.9:g.40341027G=	NCBI36
NG_008401.1:g.12414C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253408.11:c.1308C=	ENSP00000253408.5:p.Thr436=
ENST00000253408.10:c.1308C=	ENSP00000253408.5:p.Thr436=
ENST00000441312.2:n.41C=
ENST00000585543.6:n.341C=
ENST00000586125.2:c.123C=	ENSP00000467397.2:p.Thr41=
ENST00000588735.3:c.1188C= MANE Select	ENSP00000466598.2:p.Thr396=
ENST00000589701.2:n.2095C=
ENST00000591880.2:c.287C=
ENST00000592065.2:n.556C=
ENST00000638304.1:c.107C=
ENST00000638400.1:c.23C=
ENST00000638488.1:n.652C=
ENST00000638618.1:c.843C=	ENSP00000492832.1:p.Thr281=
ENST00000638921.1:n.115C=
ENST00000639042.1:c.160C=
ENST00000639277.1:c.1188C=	ENSP00000492432.1:p.Thr396=
ENST00000639369.1:c.38C=
ENST00000640859.1:c.2C=
ENST00000253408.9:c.1188C=	ENSP00000253408.4:p.Thr396=
ENST00000585543.5:n.341C=
ENST00000586125.1:c.159C=	ENSP00000467397.1:p.Thr53=
ENST00000588735.1:c.83-17C=	ENSP00000466598.1:n.83-17C=
ENST00000589701.1:n.90C=
ENST00000591880.1:c.54C=	ENSP00000467530.1:p.Thr18=
ENST00000592706.5:n.60C=
NM_002055.4:c.1188C=	NP_002046.1:p.Thr396=
NM_001363846.1:c.1308C=	NP_001350775.1:p.Thr436=
XM_024450690.1:c.1512C=	XP_024306458.1:p.Thr504=
XM_024450692.1:c.1392C=	XP_024306460.1:p.Thr464=
NM_002055.5:c.1188C= MANE Select	NP_002046.1:p.Thr396=
NM_001363846.2:c.1308C=	NP_001350775.1:p.Thr436=