Canonical Allele Identifier: CA2261612623

Gene: GFAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44913280_44913281delinsAC , CM000679.2:g.44913280_44913281delinsAC	GRCh38
NC_000017.10:g.42990648_42990649delinsAC , CM000679.1:g.42990648_42990649delinsAC	GRCh37
NC_000017.9:g.40346174_40346175delinsAC	NCBI36
NG_008401.1:g.7266_7267delinsGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000253408.11:c.768_769delinsGT	ENSP00000253408.5:p.Trp256=
ENST00000435360.8:c.768_769delinsGT	ENSP00000403962.1:p.Trp256=
ENST00000253408.10:c.768_769delinsGT	ENSP00000253408.5:p.Trp256=
ENST00000435360.7:c.768_769delinsGT	ENSP00000403962.1:p.Trp256=
ENST00000586127.6:n.1297_1298delinsGT
ENST00000586793.6:c.768_769delinsGT	ENSP00000468500.2:p.Trp256=
ENST00000587997.6:n.244_245delinsGT
ENST00000588735.3:c.768_769delinsGT MANE Select	ENSP00000466598.2:p.Trp256=
ENST00000591327.2:n.1922_1923delinsGT
ENST00000592320.6:c.618+447_618+448delinsGT	ENSP00000465320.1:n.618+447_618+448delins...
ENST00000638281.1:c.768_769delinsGT	ENSP00000491088.1:p.Trp256=
ENST00000638618.1:c.423_424delinsGT	ENSP00000492832.1:p.Trp141=
ENST00000639277.1:c.768_769delinsGT	ENSP00000492432.1:p.Trp256=
ENST00000640552.1:n.782_783delinsGT
ENST00000253408.9:c.768_769delinsGT	ENSP00000253408.4:p.Trp256=
ENST00000376990.8:c.*167_*168delinsGT	ENSP00000366189.4:n.*167_*168delinsGT
ENST00000435360.6:c.768_769delinsGT	ENSP00000403962.1:p.Trp256=
ENST00000586793.5:c.768_769delinsGT	ENSP00000468500.1:p.Trp256=
ENST00000587997.5:c.244_245delinsGT
ENST00000588316.1:c.672_673delinsGT	ENSP00000465629.1:p.Trp224=
ENST00000588735.1:c.82+2124_82+2125delinsGT	ENSP00000466598.1:n.82+2124_82+2125delins...
ENST00000588957.5:c.36_37delinsGT	ENSP00000465565.1:p.Trp12=
ENST00000590922.1:n.418_419delinsGT
ENST00000592320.5:c.618+447_618+448delinsGT	ENSP00000465320.1:n.618+447_618+448delins...
NM_001131019.2:c.768_769delinsGT	NP_001124491.1:p.Trp256=
NM_001242376.1:c.768_769delinsGT	NP_001229305.1:p.Trp256=
NM_002055.4:c.768_769delinsGT	NP_002046.1:p.Trp256=
NM_001363846.1:c.768_769delinsGT	NP_001350775.1:p.Trp256=
XM_024450690.1:c.972_973delinsGT	XP_024306458.1:p.Trp324=
XM_024450691.1:c.972_973delinsGT	XP_024306459.1:p.Trp324=
XM_024450692.1:c.972_973delinsGT	XP_024306460.1:p.Trp324=
XM_024450693.1:c.972_973delinsGT	XP_024306461.1:p.Trp324=
NM_002055.5:c.768_769delinsGT MANE Select	NP_002046.1:p.Trp256=
NM_001131019.3:c.768_769delinsGT	NP_001124491.1:p.Trp256=
NM_001242376.2:c.768_769delinsGT	NP_001229305.1:p.Trp256=
NM_001242376.3:c.768_769delinsGT	NP_001229305.1:p.Trp256=
NM_001363846.2:c.768_769delinsGT	NP_001350775.1:p.Trp256=