Canonical Allele Identifier: CA500321453
Gene: GFAP HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.42990640G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44913272G>A , CM000679.2:g.44913272G>A GRCh38
NC_000017.10:g.42990640G>A , CM000679.1:g.42990640G>A GRCh37
NC_000017.9:g.40346166G>A NCBI36
NG_008401.1:g.7275C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000253408.11:c.777C>T ENSP00000253408.5:p.Ser259=
ENST00000435360.8:c.777C>T ENSP00000403962.1:p.Ser259=
ENST00000253408.10:c.777C>T ENSP00000253408.5:p.Ser259=
ENST00000435360.7:c.777C>T ENSP00000403962.1:p.Ser259=
ENST00000586127.6:n.1306C>T
ENST00000586793.6:c.777C>T ENSP00000468500.2:p.Ser259=
ENST00000587997.6:n.253C>T
ENST00000588735.3:c.777C>T MANE Select ENSP00000466598.2:p.Ser259=
ENST00000591327.2:n.1931C>T
ENST00000592320.6:c.618+456C>T ENSP00000465320.1:n.618+456C>T
ENST00000638281.1:c.777C>T ENSP00000491088.1:p.Ser259=
ENST00000638618.1:c.432C>T ENSP00000492832.1:p.Ser144=
ENST00000639277.1:c.777C>T ENSP00000492432.1:p.Ser259=
ENST00000640552.1:n.791C>T
ENST00000253408.9:c.777C>T ENSP00000253408.4:p.Ser259=
ENST00000376990.8:c.*176C>T ENSP00000366189.4:n.*176C>T
ENST00000435360.6:c.777C>T ENSP00000403962.1:p.Ser259=
ENST00000586793.5:c.777C>T ENSP00000468500.1:p.Ser259=
ENST00000587997.5:c.253C>T
ENST00000588316.1:c.681C>T ENSP00000465629.1:p.Ser227=
ENST00000588735.1:c.82+2133C>T ENSP00000466598.1:n.82+2133C>T
ENST00000588957.5:c.45C>T ENSP00000465565.1:p.Ser15=
ENST00000590922.1:n.427C>T
ENST00000592320.5:c.618+456C>T ENSP00000465320.1:n.618+456C>T
NM_001131019.2:c.777C>T NP_001124491.1:p.Ser259=
NM_001242376.1:c.777C>T NP_001229305.1:p.Ser259=
NM_002055.4:c.777C>T NP_002046.1:p.Ser259=
NM_001363846.1:c.777C>T NP_001350775.1:p.Ser259=
XM_024450690.1:c.981C>T XP_024306458.1:p.Ser327=
XM_024450691.1:c.981C>T XP_024306459.1:p.Ser327=
XM_024450692.1:c.981C>T XP_024306460.1:p.Ser327=
XM_024450693.1:c.981C>T XP_024306461.1:p.Ser327=
NM_002055.5:c.777C>T MANE Select NP_002046.1:p.Ser259=
NM_001131019.3:c.777C>T NP_001124491.1:p.Ser259=
NM_001242376.2:c.777C>T NP_001229305.1:p.Ser259=
NM_001242376.3:c.777C>T NP_001229305.1:p.Ser259=
NM_001363846.2:c.777C>T NP_001350775.1:p.Ser259=