Canonical Allele Identifier: CA500321293
Gene: GFAP HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.42988699G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44911331G>A , CM000679.2:g.44911331G>A GRCh38
NC_000017.10:g.42988699G>A , CM000679.1:g.42988699G>A GRCh37
NC_000017.9:g.40344225G>A NCBI36
NG_008401.1:g.9216C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000253408.11:c.1032C>T ENSP00000253408.5:p.Arg344=
ENST00000435360.8:c.1032C>T ENSP00000403962.1:p.Arg344=
ENST00000253408.10:c.1032C>T ENSP00000253408.5:p.Arg344=
ENST00000435360.7:c.1032C>T ENSP00000403962.1:p.Arg344=
ENST00000585543.6:n.185C>T
ENST00000586127.6:n.1561C>T
ENST00000586793.6:c.907-10C>T ENSP00000468500.2:n.907-10C>T
ENST00000587997.6:n.508C>T
ENST00000588735.3:c.1032C>T MANE Select ENSP00000466598.2:p.Arg344=
ENST00000591327.2:n.2186C>T
ENST00000592320.6:c.619-10C>T ENSP00000465320.1:n.619-10C>T
ENST00000638281.1:c.1032C>T ENSP00000491088.1:p.Arg344=
ENST00000638618.1:c.687C>T ENSP00000492832.1:p.Arg229=
ENST00000639277.1:c.1032C>T ENSP00000492432.1:p.Arg344=
ENST00000640552.1:n.1046C>T
ENST00000253408.9:c.1032C>T ENSP00000253408.4:p.Arg344=
ENST00000376990.8:c.*431C>T ENSP00000366189.4:n.*431C>T
ENST00000435360.6:c.1032C>T ENSP00000403962.1:p.Arg344=
ENST00000585543.5:n.185C>T
ENST00000586793.5:c.1032C>T ENSP00000468500.1:p.Arg344=
ENST00000587997.5:c.508C>T
ENST00000588640.5:n.412C>T
ENST00000588735.1:c.83-3215C>T ENSP00000466598.1:n.83-3215C>T
ENST00000592320.5:c.619-10C>T ENSP00000465320.1:n.619-10C>T
NM_001131019.2:c.1032C>T NP_001124491.1:p.Arg344=
NM_001242376.1:c.1032C>T NP_001229305.1:p.Arg344=
NM_002055.4:c.1032C>T NP_002046.1:p.Arg344=
NM_001363846.1:c.1032C>T NP_001350775.1:p.Arg344=
XM_024450690.1:c.1236C>T XP_024306458.1:p.Arg412=
XM_024450691.1:c.1236C>T XP_024306459.1:p.Arg412=
XM_024450692.1:c.1236C>T XP_024306460.1:p.Arg412=
XM_024450693.1:c.1236C>T XP_024306461.1:p.Arg412=
NM_002055.5:c.1032C>T MANE Select NP_002046.1:p.Arg344=
NM_001131019.3:c.1032C>T NP_001124491.1:p.Arg344=
NM_001242376.2:c.1032C>T NP_001229305.1:p.Arg344=
NM_001242376.3:c.1032C>T NP_001229305.1:p.Arg344=
NM_001363846.2:c.1032C>T NP_001350775.1:p.Arg344=