Canonical Allele Identifier: CA8608779

Gene: GFAP

Linked Data

• ClinVar Variation Id: 1900837
• ClinVar RCV Id: RCV002585942
• dbSNP Id: rs767003792
• ExAC: 17:42988759 A / G
• gnomAD v2: 17-42988759-A-G
• gnomAD v4: 17-44911391-A-G
• MyVariant Identifiers: chr17:g.42988759A>G (hg19) ; chr17:g.44911391A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44911391A>G , CM000679.2:g.44911391A>G	GRCh38
NC_000017.10:g.42988759A>G , CM000679.1:g.42988759A>G	GRCh37
NC_000017.9:g.40344285A>G	NCBI36
NG_008401.1:g.9156T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000253408.11:c.972T>C	ENSP00000253408.5:p.Tyr324=
ENST00000435360.8:c.972T>C	ENSP00000403962.1:p.Tyr324=
ENST00000253408.10:c.972T>C	ENSP00000253408.5:p.Tyr324=
ENST00000435360.7:c.972T>C	ENSP00000403962.1:p.Tyr324=
ENST00000585543.6:n.125T>C
ENST00000586127.6:n.1501T>C
ENST00000586793.6:c.907-70T>C	ENSP00000468500.2:n.907-70T>C
ENST00000587997.6:n.448T>C
ENST00000588735.3:c.972T>C MANE Select	ENSP00000466598.2:p.Tyr324=
ENST00000591327.2:n.2126T>C
ENST00000592320.6:c.619-70T>C	ENSP00000465320.1:n.619-70T>C
ENST00000638281.1:c.972T>C	ENSP00000491088.1:p.Tyr324=
ENST00000638618.1:c.627T>C	ENSP00000492832.1:p.Tyr209=
ENST00000639277.1:c.972T>C	ENSP00000492432.1:p.Tyr324=
ENST00000640552.1:n.986T>C
ENST00000253408.9:c.972T>C	ENSP00000253408.4:p.Tyr324=
ENST00000376990.8:c.*371T>C	ENSP00000366189.4:n.*371T>C
ENST00000435360.6:c.972T>C	ENSP00000403962.1:p.Tyr324=
ENST00000585543.5:n.125T>C
ENST00000586793.5:c.972T>C	ENSP00000468500.1:p.Tyr324=
ENST00000587997.5:c.448T>C
ENST00000588640.5:n.352T>C
ENST00000588735.1:c.83-3275T>C	ENSP00000466598.1:n.83-3275T>C
ENST00000592320.5:c.619-70T>C	ENSP00000465320.1:n.619-70T>C
NM_001131019.2:c.972T>C	NP_001124491.1:p.Tyr324=
NM_001242376.1:c.972T>C	NP_001229305.1:p.Tyr324=
NM_002055.4:c.972T>C	NP_002046.1:p.Tyr324=
NM_001363846.1:c.972T>C	NP_001350775.1:p.Tyr324=
XM_024450690.1:c.1176T>C	XP_024306458.1:p.Tyr392=
XM_024450691.1:c.1176T>C	XP_024306459.1:p.Tyr392=
XM_024450692.1:c.1176T>C	XP_024306460.1:p.Tyr392=
XM_024450693.1:c.1176T>C	XP_024306461.1:p.Tyr392=
NM_002055.5:c.972T>C MANE Select	NP_002046.1:p.Tyr324=
NM_001131019.3:c.972T>C	NP_001124491.1:p.Tyr324=
NM_001242376.2:c.972T>C	NP_001229305.1:p.Tyr324=
NM_001242376.3:c.972T>C	NP_001229305.1:p.Tyr324=
NM_001363846.2:c.972T>C	NP_001350775.1:p.Tyr324=