Canonical Allele Identifier: CA2261613759

Gene: GFAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44915518G= , CM000679.2:g.44915518G=	GRCh38
NC_000017.10:g.42992886G= , CM000679.1:g.42992886G=	GRCh37
NC_000017.9:g.40348412G=	NCBI36
NG_008401.1:g.5029C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253408.9:c.-32C=	ENSP00000253408.4:n.-32C=
ENST00000588957.5:c.-272+299C=	ENSP00000465565.1:n.-272+299C=
ENST00000593179.1:c.-22-10C=	ENSP00000467106.1:n.-22-10C=
NM_001131019.2:c.-32C=	NP_001124491.1:n.-32C=
NM_001242376.1:c.-32C=	NP_001229305.1:n.-32C=
NM_002055.4:c.-32C=	NP_002046.1:n.-32C=
NM_001363846.1:c.-32C=	NP_001350775.1:n.-32C=
XM_024450690.1:c.-32C=	XP_024306458.1:n.-32C=
XM_024450691.1:c.-32C=	XP_024306459.1:n.-32C=
XM_024450692.1:c.-32C=	XP_024306460.1:n.-32C=
XM_024450693.1:c.-32C=	XP_024306461.1:n.-32C=