Canonical Allele Identifier: CA2261613754

Gene: GFAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44915506C= , CM000679.2:g.44915506C=	GRCh38
NC_000017.10:g.42992874C= , CM000679.1:g.42992874C=	GRCh37
NC_000017.9:g.40348400C=	NCBI36
NG_008401.1:g.5041G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253408.9:c.-20G=	ENSP00000253408.4:n.-20G=
ENST00000588957.5:c.-272+311G=	ENSP00000465565.1:n.-272+311G=
ENST00000593179.1:c.-20G=	ENSP00000467106.1:n.-20G=
NM_001131019.2:c.-20G=	NP_001124491.1:n.-20G=
NM_001242376.1:c.-20G=	NP_001229305.1:n.-20G=
NM_002055.4:c.-20G=	NP_002046.1:n.-20G=
NM_001363846.1:c.-20G=	NP_001350775.1:n.-20G=
XM_024450690.1:c.-20G=	XP_024306458.1:n.-20G=
XM_024450691.1:c.-20G=	XP_024306459.1:n.-20G=
XM_024450692.1:c.-20G=	XP_024306460.1:n.-20G=
XM_024450693.1:c.-20G=	XP_024306461.1:n.-20G=