Canonical Allele Identifier: CA500321255

Gene: GFAP

Linked Data

• MyVariant Identifiers: chr17:g.42988639G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44911271G>A , CM000679.2:g.44911271G>A	GRCh38
NC_000017.10:g.42988639G>A , CM000679.1:g.42988639G>A	GRCh37
NC_000017.9:g.40344165G>A	NCBI36
NG_008401.1:g.9276C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000253408.11:c.1092C>T	ENSP00000253408.5:p.Ala364=
ENST00000435360.8:c.1092C>T	ENSP00000403962.1:p.Ala364=
ENST00000253408.10:c.1092C>T	ENSP00000253408.5:p.Ala364=
ENST00000435360.7:c.1092C>T	ENSP00000403962.1:p.Ala364=
ENST00000585543.6:n.245C>T
ENST00000586125.2:c.27C>T	ENSP00000467397.2:p.Ala9=
ENST00000586127.6:n.1621C>T
ENST00000586793.6:c.957C>T	ENSP00000468500.2:p.Ala319=
ENST00000587997.6:n.568C>T
ENST00000588735.3:c.1092C>T MANE Select	ENSP00000466598.2:p.Ala364=
ENST00000591327.2:n.2246C>T
ENST00000591880.2:c.22C>T
ENST00000592320.6:c.669C>T	ENSP00000465320.1:p.Ala223=
ENST00000638281.1:c.1092C>T	ENSP00000491088.1:p.Ala364=
ENST00000638304.1:c.11C>T
ENST00000638488.1:n.33C>T
ENST00000638618.1:c.747C>T	ENSP00000492832.1:p.Ala249=
ENST00000639042.1:c.29C>T
ENST00000639277.1:c.1092C>T	ENSP00000492432.1:p.Ala364=
ENST00000639921.1:c.49C>T
ENST00000640552.1:n.1106C>T
ENST00000253408.9:c.1092C>T	ENSP00000253408.4:p.Ala364=
ENST00000435360.6:c.1092C>T	ENSP00000403962.1:p.Ala364=
ENST00000585543.5:n.245C>T
ENST00000586793.5:c.1092C>T	ENSP00000468500.1:p.Ala364=
ENST00000587997.5:c.568C>T
ENST00000588640.5:n.472C>T
ENST00000588735.1:c.83-3155C>T	ENSP00000466598.1:n.83-3155C>T
ENST00000592320.5:c.669C>T	ENSP00000465320.1:p.Ala223=
NM_001131019.2:c.1092C>T	NP_001124491.1:p.Ala364=
NM_001242376.1:c.1092C>T	NP_001229305.1:p.Ala364=
NM_002055.4:c.1092C>T	NP_002046.1:p.Ala364=
NM_001363846.1:c.1092C>T	NP_001350775.1:p.Ala364=
XM_024450690.1:c.1296C>T	XP_024306458.1:p.Ala432=
XM_024450691.1:c.1296C>T	XP_024306459.1:p.Ala432=
XM_024450692.1:c.1296C>T	XP_024306460.1:p.Ala432=
XM_024450693.1:c.1296C>T	XP_024306461.1:p.Ala432=
NM_002055.5:c.1092C>T MANE Select	NP_002046.1:p.Ala364=
NM_001131019.3:c.1092C>T	NP_001124491.1:p.Ala364=
NM_001242376.2:c.1092C>T	NP_001229305.1:p.Ala364=
NM_001242376.3:c.1092C>T	NP_001229305.1:p.Ala364=
NM_001363846.2:c.1092C>T	NP_001350775.1:p.Ala364=