Canonical Allele Identifier: CA2261610332

Gene: GFAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44908298G= , CM000679.2:g.44908298G=	GRCh38
NC_000017.10:g.42985666G= , CM000679.1:g.42985666G=	GRCh37
NC_000017.9:g.40341192G=	NCBI36
NG_008401.1:g.12249C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253408.11:c.1292-149C=	ENSP00000253408.5:n.1292-149C=
ENST00000253408.10:c.1292-149C=	ENSP00000253408.5:n.1292-149C=
ENST00000441312.2:n.25-149C=
ENST00000585543.6:n.325-149C=
ENST00000586125.2:c.107-149C=	ENSP00000467397.2:n.107-149C=
ENST00000588735.3:c.1172-149C= MANE Select	ENSP00000466598.2:n.1172-149C=
ENST00000589701.2:n.1930C=
ENST00000591880.2:c.271-149C=
ENST00000592065.2:n.391C=
ENST00000638304.1:c.91-149C=
ENST00000638400.1:c.7-149C=
ENST00000638488.1:n.636-149C=
ENST00000638618.1:c.827-149C=	ENSP00000492832.1:n.827-149C=
ENST00000639042.1:c.144-149C=
ENST00000639277.1:c.1172-149C=	ENSP00000492432.1:n.1172-149C=
ENST00000639369.1:c.22-149C=
ENST00000640552.1:n.3502C=
ENST00000253408.9:c.1172-149C=	ENSP00000253408.4:n.1172-149C=
ENST00000585543.5:n.325-149C=
ENST00000586125.1:c.143-149C=	ENSP00000467397.1:n.143-149C=
ENST00000588640.5:n.552-149C=
ENST00000588735.1:c.83-182C=	ENSP00000466598.1:n.83-182C=
ENST00000591880.1:c.38-149C=	ENSP00000467530.1:n.38-149C=
ENST00000592706.5:n.44-149C=
NM_002055.4:c.1172-149C=	NP_002046.1:n.1172-149C=
NM_001363846.1:c.1292-149C=	NP_001350775.1:n.1292-149C=
XM_024450690.1:c.1496-149C=	XP_024306458.1:n.1496-149C=
XM_024450692.1:c.1376-149C=	XP_024306460.1:n.1376-149C=
NM_002055.5:c.1172-149C= MANE Select	NP_002046.1:n.1172-149C=
NM_001242376.2:c.*2171C=	NP_001229305.1:n.*2171C=
NM_001363846.2:c.1292-149C=	NP_001350775.1:n.1292-149C=