Canonical Allele Identifier: CA984042479

Gene: GFAP

Linked Data

• dbSNP Id: rs2051764776
• gnomAD v3: 17-44911486-A-G
• gnomAD v4: 17-44911486-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44911486A>G , CM000679.2:g.44911486A>G	GRCh38
NC_000017.10:g.42988854A>G , CM000679.1:g.42988854A>G	GRCh37
NC_000017.9:g.40344380A>G	NCBI36
NG_008401.1:g.9061T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253408.11:c.907-30T>C	ENSP00000253408.5:n.907-30T>C
ENST00000435360.8:c.907-30T>C	ENSP00000403962.1:n.907-30T>C
ENST00000253408.10:c.907-30T>C	ENSP00000253408.5:n.907-30T>C
ENST00000435360.7:c.907-30T>C	ENSP00000403962.1:n.907-30T>C
ENST00000585543.6:n.30T>C
ENST00000586127.6:n.1436-30T>C
ENST00000586793.6:c.907-165T>C	ENSP00000468500.2:n.907-165T>C
ENST00000587997.6:n.383-30T>C
ENST00000588735.3:c.907-30T>C MANE Select	ENSP00000466598.2:n.907-30T>C
ENST00000591327.2:n.2061-30T>C
ENST00000592320.6:c.619-165T>C	ENSP00000465320.1:n.619-165T>C
ENST00000638281.1:c.907-30T>C	ENSP00000491088.1:n.907-30T>C
ENST00000638618.1:c.562-30T>C	ENSP00000492832.1:n.562-30T>C
ENST00000639277.1:c.907-30T>C	ENSP00000492432.1:n.907-30T>C
ENST00000640552.1:n.921-30T>C
ENST00000253408.9:c.907-30T>C	ENSP00000253408.4:n.907-30T>C
ENST00000376990.8:c.*306-30T>C	ENSP00000366189.4:n.*306-30T>C
ENST00000435360.6:c.907-30T>C	ENSP00000403962.1:n.907-30T>C
ENST00000585543.5:n.30T>C
ENST00000586793.5:c.907-30T>C	ENSP00000468500.1:n.907-30T>C
ENST00000587997.5:c.383-30T>C
ENST00000588640.5:n.287-30T>C
ENST00000588735.1:c.83-3370T>C	ENSP00000466598.1:n.83-3370T>C
ENST00000591719.5:n.541-30T>C
ENST00000592320.5:c.619-165T>C	ENSP00000465320.1:n.619-165T>C
NM_001131019.2:c.907-30T>C	NP_001124491.1:n.907-30T>C
NM_001242376.1:c.907-30T>C	NP_001229305.1:n.907-30T>C
NM_002055.4:c.907-30T>C	NP_002046.1:n.907-30T>C
NM_001363846.1:c.907-30T>C	NP_001350775.1:n.907-30T>C
XM_024450690.1:c.1111-30T>C	XP_024306458.1:n.1111-30T>C
XM_024450691.1:c.1111-30T>C	XP_024306459.1:n.1111-30T>C
XM_024450692.1:c.1111-30T>C	XP_024306460.1:n.1111-30T>C
XM_024450693.1:c.1111-30T>C	XP_024306461.1:n.1111-30T>C
NM_002055.5:c.907-30T>C MANE Select	NP_002046.1:n.907-30T>C
NM_001131019.3:c.907-30T>C	NP_001124491.1:n.907-30T>C
NM_001242376.2:c.907-30T>C	NP_001229305.1:n.907-30T>C
NM_001242376.3:c.907-30T>C	NP_001229305.1:n.907-30T>C
NM_001363846.2:c.907-30T>C	NP_001350775.1:n.907-30T>C