Canonical Allele Identifier: CA347188

Gene: GFAP

Linked Data

• ClinVar Variation Id: 190337
• ClinVar RCV Id: RCV000192113
• dbSNP Id: rs797044572
• MyVariant Identifiers: chr17:g.42992616A>G (hg19) ; chr17:g.44915248A>G (hg38)
• PubMed: PMID:20301351 ; PMID:24045243

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44915248A>G , CM000679.2:g.44915248A>G	GRCh38
NC_000017.10:g.42992616A>G , CM000679.1:g.42992616A>G	GRCh37
NC_000017.9:g.40348142A>G	NCBI36
NG_008401.1:g.5299T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253408.11:c.239T>C	ENSP00000253408.5:p.Phe80Ser
ENST00000435360.8:c.239T>C	ENSP00000403962.1:p.Phe80Ser
ENST00000253408.10:c.239T>C	ENSP00000253408.5:p.Phe80Ser
ENST00000435360.7:c.239T>C	ENSP00000403962.1:p.Phe80Ser
ENST00000586793.6:c.239T>C	ENSP00000468500.2:p.Phe80Ser
ENST00000588735.3:c.239T>C MANE Select	ENSP00000466598.2:p.Phe80Ser
ENST00000591327.2:n.252T>C
ENST00000592320.6:c.239T>C	ENSP00000465320.1:p.Phe80Ser
ENST00000638281.1:c.239T>C	ENSP00000491088.1:p.Phe80Ser
ENST00000639277.1:c.239T>C	ENSP00000492432.1:p.Phe80Ser
ENST00000640552.1:n.253T>C
ENST00000253408.9:c.239T>C	ENSP00000253408.4:p.Phe80Ser
ENST00000376990.8:c.239T>C	ENSP00000366189.4:p.Phe80Ser
ENST00000435360.6:c.239T>C	ENSP00000403962.1:p.Phe80Ser
ENST00000585728.5:c.181+58T>C	ENSP00000465208.1:n.181+58T>C
ENST00000586793.5:c.239T>C	ENSP00000468500.1:p.Phe80Ser
ENST00000588037.1:c.239T>C	ENSP00000466163.1:p.Phe80Ser
ENST00000588316.1:c.239T>C	ENSP00000465629.1:p.Phe80Ser
ENST00000588735.1:c.82+157T>C	ENSP00000466598.1:n.82+157T>C
ENST00000588957.5:c.-272+569T>C	ENSP00000465565.1:n.-272+569T>C
ENST00000591327.1:n.253T>C
ENST00000592320.5:c.239T>C	ENSP00000465320.1:p.Phe80Ser
NM_001131019.2:c.239T>C	NP_001124491.1:p.Phe80Ser
NM_001242376.1:c.239T>C	NP_001229305.1:p.Phe80Ser
NM_002055.4:c.239T>C	NP_002046.1:p.Phe80Ser
NM_001363846.1:c.239T>C	NP_001350775.1:p.Phe80Ser
XM_024450690.1:c.239T>C	XP_024306458.1:p.Phe80Ser
XM_024450691.1:c.239T>C	XP_024306459.1:p.Phe80Ser
XM_024450692.1:c.239T>C	XP_024306460.1:p.Phe80Ser
XM_024450693.1:c.239T>C	XP_024306461.1:p.Phe80Ser
NM_002055.5:c.239T>C MANE Select	NP_002046.1:p.Phe80Ser
NM_001131019.3:c.239T>C	NP_001124491.1:p.Phe80Ser
NM_001242376.2:c.239T>C	NP_001229305.1:p.Phe80Ser
NM_001242376.3:c.239T>C	NP_001229305.1:p.Phe80Ser
NM_001363846.2:c.239T>C	NP_001350775.1:p.Phe80Ser