Canonical Allele Identifier: CA2261613751

Gene: GFAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44915501G= , CM000679.2:g.44915501G=	GRCh38
NC_000017.10:g.42992869G= , CM000679.1:g.42992869G=	GRCh37
NC_000017.9:g.40348395G=	NCBI36
NG_008401.1:g.5046C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592320.6:c.-15C=	ENSP00000465320.1:n.-15C=
ENST00000253408.9:c.-15C=	ENSP00000253408.4:n.-15C=
ENST00000588037.1:c.-15C=	ENSP00000466163.1:n.-15C=
ENST00000588957.5:c.-272+316C=	ENSP00000465565.1:n.-272+316C=
ENST00000592320.5:c.-15C=	ENSP00000465320.1:n.-15C=
ENST00000593179.1:c.-15C=	ENSP00000467106.1:n.-15C=
NM_001131019.2:c.-15C=	NP_001124491.1:n.-15C=
NM_001242376.1:c.-15C=	NP_001229305.1:n.-15C=
NM_002055.4:c.-15C=	NP_002046.1:n.-15C=
NM_001363846.1:c.-15C=	NP_001350775.1:n.-15C=
XM_024450690.1:c.-15C=	XP_024306458.1:n.-15C=
XM_024450691.1:c.-15C=	XP_024306459.1:n.-15C=
XM_024450692.1:c.-15C=	XP_024306460.1:n.-15C=
XM_024450693.1:c.-15C=	XP_024306461.1:n.-15C=