Canonical Allele Identifier: CA2733868698
Gene: GFAP HGNC NCBI

Linked Data

dbSNP Id: rs2145643616

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44915515dup , CM000679.2:g.44915515dup GRCh38
NC_000017.10:g.42992883dup , CM000679.1:g.42992883dup GRCh37
NC_000017.9:g.40348409dup NCBI36
NG_008401.1:g.5032dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000253408.9:c.-29dup ENSP00000253408.4:n.-29dup
ENST00000588957.5:c.-272+302dup ENSP00000465565.1:n.-272+302dup
ENST00000593179.1:c.-22-7dup ENSP00000467106.1:n.-22-7dup
NM_001131019.2:c.-29dup NP_001124491.1:n.-29dup
NM_001242376.1:c.-29dup NP_001229305.1:n.-29dup
NM_002055.4:c.-29dup NP_002046.1:n.-29dup
NM_001363846.1:c.-29dup NP_001350775.1:n.-29dup
XM_024450690.1:c.-29dup XP_024306458.1:n.-29dup
XM_024450691.1:c.-29dup XP_024306459.1:n.-29dup
XM_024450692.1:c.-29dup XP_024306460.1:n.-29dup
XM_024450693.1:c.-29dup XP_024306461.1:n.-29dup