Canonical Allele Identifier: CA399845859

Gene: GFAP

Linked Data

• MyVariant Identifiers: chr17:g.42990743T>A (hg19) ; chr17:g.44913375T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44913375T>A , CM000679.2:g.44913375T>A	GRCh38
NC_000017.10:g.42990743T>A , CM000679.1:g.42990743T>A	GRCh37
NC_000017.9:g.40346269T>A	NCBI36
NG_008401.1:g.7172A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253408.11:c.674A>T	ENSP00000253408.5:p.Asp225Val
ENST00000435360.8:c.674A>T	ENSP00000403962.1:p.Asp225Val
ENST00000253408.10:c.674A>T	ENSP00000253408.5:p.Asp225Val
ENST00000435360.7:c.674A>T	ENSP00000403962.1:p.Asp225Val
ENST00000586127.6:n.1203A>T
ENST00000586793.6:c.674A>T	ENSP00000468500.2:p.Asp225Val
ENST00000587997.6:n.150A>T
ENST00000588735.3:c.674A>T MANE Select	ENSP00000466598.2:p.Asp225Val
ENST00000591327.2:n.1828A>T
ENST00000592320.6:c.618+353A>T	ENSP00000465320.1:n.618+353A>T
ENST00000638281.1:c.674A>T	ENSP00000491088.1:p.Asp225Val
ENST00000638618.1:c.329A>T	ENSP00000492832.1:p.Asp110Val
ENST00000639277.1:c.674A>T	ENSP00000492432.1:p.Asp225Val
ENST00000640552.1:n.688A>T
ENST00000253408.9:c.674A>T	ENSP00000253408.4:p.Asp225Val
ENST00000376990.8:c.*73A>T	ENSP00000366189.4:n.*73A>T
ENST00000435360.6:c.674A>T	ENSP00000403962.1:p.Asp225Val
ENST00000585728.5:c.*318A>T	ENSP00000465208.1:n.*318A>T
ENST00000586127.5:c.13A>T	ENSP00000464795.1:p.Thr5Ser
ENST00000586793.5:c.674A>T	ENSP00000468500.1:p.Asp225Val
ENST00000587997.5:c.150A>T
ENST00000588316.1:c.578A>T	ENSP00000465629.1:p.Asp193Val
ENST00000588735.1:c.82+2030A>T	ENSP00000466598.1:n.82+2030A>T
ENST00000588957.5:c.-59A>T	ENSP00000465565.1:n.-59A>T
ENST00000590922.1:n.324A>T
ENST00000592320.5:c.618+353A>T	ENSP00000465320.1:n.618+353A>T
NM_001131019.2:c.674A>T	NP_001124491.1:p.Asp225Val
NM_001242376.1:c.674A>T	NP_001229305.1:p.Asp225Val
NM_002055.4:c.674A>T	NP_002046.1:p.Asp225Val
NM_001363846.1:c.674A>T	NP_001350775.1:p.Asp225Val
XM_024450690.1:c.878A>T	XP_024306458.1:p.Asp293Val
XM_024450691.1:c.878A>T	XP_024306459.1:p.Asp293Val
XM_024450692.1:c.878A>T	XP_024306460.1:p.Asp293Val
XM_024450693.1:c.878A>T	XP_024306461.1:p.Asp293Val
NM_002055.5:c.674A>T MANE Select	NP_002046.1:p.Asp225Val
NM_001131019.3:c.674A>T	NP_001124491.1:p.Asp225Val
NM_001242376.2:c.674A>T	NP_001229305.1:p.Asp225Val
NM_001242376.3:c.674A>T	NP_001229305.1:p.Asp225Val
NM_001363846.2:c.674A>T	NP_001350775.1:p.Asp225Val