Canonical Allele Identifier: CA2261610317

Gene: GFAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44908250T= , CM000679.2:g.44908250T=	GRCh38
NC_000017.10:g.42985618T= , CM000679.1:g.42985618T=	GRCh37
NC_000017.9:g.40341144T=	NCBI36
NG_008401.1:g.12297A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253408.11:c.1292-101A=	ENSP00000253408.5:n.1292-101A=
ENST00000253408.10:c.1292-101A=	ENSP00000253408.5:n.1292-101A=
ENST00000441312.2:n.25-101A=
ENST00000585543.6:n.325-101A=
ENST00000586125.2:c.107-101A=	ENSP00000467397.2:n.107-101A=
ENST00000588735.3:c.1172-101A= MANE Select	ENSP00000466598.2:n.1172-101A=
ENST00000589701.2:n.1978A=
ENST00000591880.2:c.271-101A=
ENST00000592065.2:n.439A=
ENST00000638304.1:c.91-101A=
ENST00000638400.1:c.7-101A=
ENST00000638488.1:n.636-101A=
ENST00000638618.1:c.827-101A=	ENSP00000492832.1:n.827-101A=
ENST00000639042.1:c.144-101A=
ENST00000639277.1:c.1172-101A=	ENSP00000492432.1:n.1172-101A=
ENST00000639369.1:c.22-101A=
ENST00000640552.1:n.3550A=
ENST00000253408.9:c.1172-101A=	ENSP00000253408.4:n.1172-101A=
ENST00000585543.5:n.325-101A=
ENST00000586125.1:c.143-101A=	ENSP00000467397.1:n.143-101A=
ENST00000588640.5:n.552-101A=
ENST00000588735.1:c.83-134A=	ENSP00000466598.1:n.83-134A=
ENST00000591880.1:c.38-101A=	ENSP00000467530.1:n.38-101A=
ENST00000592706.5:n.44-101A=
NM_002055.4:c.1172-101A=	NP_002046.1:n.1172-101A=
NM_001363846.1:c.1292-101A=	NP_001350775.1:n.1292-101A=
XM_024450690.1:c.1496-101A=	XP_024306458.1:n.1496-101A=
XM_024450692.1:c.1376-101A=	XP_024306460.1:n.1376-101A=
NM_002055.5:c.1172-101A= MANE Select	NP_002046.1:n.1172-101A=
NM_001242376.2:c.*2219A=	NP_001229305.1:n.*2219A=
NM_001363846.2:c.1292-101A=	NP_001350775.1:n.1292-101A=