Canonical Allele Identifier: CA399845669

Gene: GFAP

Linked Data

• MyVariant Identifiers: chr17:g.42990687C>A (hg19) ; chr17:g.44913319C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44913319C>A , CM000679.2:g.44913319C>A	GRCh38
NC_000017.10:g.42990687C>A , CM000679.1:g.42990687C>A	GRCh37
NC_000017.9:g.40346213C>A	NCBI36
NG_008401.1:g.7228G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253408.11:c.730G>T	ENSP00000253408.5:p.Ala244Ser
ENST00000435360.8:c.730G>T	ENSP00000403962.1:p.Ala244Ser
ENST00000253408.10:c.730G>T	ENSP00000253408.5:p.Ala244Ser
ENST00000435360.7:c.730G>T	ENSP00000403962.1:p.Ala244Ser
ENST00000586127.6:n.1259G>T
ENST00000586793.6:c.730G>T	ENSP00000468500.2:p.Ala244Ser
ENST00000587997.6:n.206G>T
ENST00000588735.3:c.730G>T MANE Select	ENSP00000466598.2:p.Ala244Ser
ENST00000591327.2:n.1884G>T
ENST00000592320.6:c.618+409G>T	ENSP00000465320.1:n.618+409G>T
ENST00000638281.1:c.730G>T	ENSP00000491088.1:p.Ala244Ser
ENST00000638618.1:c.385G>T	ENSP00000492832.1:p.Ala129Ser
ENST00000639277.1:c.730G>T	ENSP00000492432.1:p.Ala244Ser
ENST00000640552.1:n.744G>T
ENST00000253408.9:c.730G>T	ENSP00000253408.4:p.Ala244Ser
ENST00000376990.8:c.*129G>T	ENSP00000366189.4:n.*129G>T
ENST00000435360.6:c.730G>T	ENSP00000403962.1:p.Ala244Ser
ENST00000585728.5:c.*374G>T	ENSP00000465208.1:n.*374G>T
ENST00000586793.5:c.730G>T	ENSP00000468500.1:p.Ala244Ser
ENST00000587997.5:c.206G>T
ENST00000588316.1:c.634G>T	ENSP00000465629.1:p.Ala212Ser
ENST00000588735.1:c.82+2086G>T	ENSP00000466598.1:n.82+2086G>T
ENST00000588957.5:c.-3G>T	ENSP00000465565.1:n.-3G>T
ENST00000590922.1:n.380G>T
ENST00000592320.5:c.618+409G>T	ENSP00000465320.1:n.618+409G>T
NM_001131019.2:c.730G>T	NP_001124491.1:p.Ala244Ser
NM_001242376.1:c.730G>T	NP_001229305.1:p.Ala244Ser
NM_002055.4:c.730G>T	NP_002046.1:p.Ala244Ser
NM_001363846.1:c.730G>T	NP_001350775.1:p.Ala244Ser
XM_024450690.1:c.934G>T	XP_024306458.1:p.Ala312Ser
XM_024450691.1:c.934G>T	XP_024306459.1:p.Ala312Ser
XM_024450692.1:c.934G>T	XP_024306460.1:p.Ala312Ser
XM_024450693.1:c.934G>T	XP_024306461.1:p.Ala312Ser
NM_002055.5:c.730G>T MANE Select	NP_002046.1:p.Ala244Ser
NM_001131019.3:c.730G>T	NP_001124491.1:p.Ala244Ser
NM_001242376.2:c.730G>T	NP_001229305.1:p.Ala244Ser
NM_001242376.3:c.730G>T	NP_001229305.1:p.Ala244Ser
NM_001363846.2:c.730G>T	NP_001350775.1:p.Ala244Ser