Canonical Allele Identifier: CA2261613753
Gene: GFAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44915505G= , CM000679.2:g.44915505G= GRCh38
NC_000017.10:g.42992873G= , CM000679.1:g.42992873G= GRCh37
NC_000017.9:g.40348399G= NCBI36
NG_008401.1:g.5042C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000253408.9:c.-19C= ENSP00000253408.4:n.-19C=
ENST00000588957.5:c.-272+312C= ENSP00000465565.1:n.-272+312C=
ENST00000593179.1:c.-19C= ENSP00000467106.1:n.-19C=
NM_001131019.2:c.-19C= NP_001124491.1:n.-19C=
NM_001242376.1:c.-19C= NP_001229305.1:n.-19C=
NM_002055.4:c.-19C= NP_002046.1:n.-19C=
NM_001363846.1:c.-19C= NP_001350775.1:n.-19C=
XM_024450690.1:c.-19C= XP_024306458.1:n.-19C=
XM_024450691.1:c.-19C= XP_024306459.1:n.-19C=
XM_024450692.1:c.-19C= XP_024306460.1:n.-19C=
XM_024450693.1:c.-19C= XP_024306461.1:n.-19C=