Canonical Allele Identifier: CA2638278260

Gene: GFAP

Linked Data

• gnomAD v4: 17-44915508-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44915508C>G , CM000679.2:g.44915508C>G	GRCh38
NC_000017.10:g.42992876C>G , CM000679.1:g.42992876C>G	GRCh37
NC_000017.9:g.40348402C>G	NCBI36
NG_008401.1:g.5039G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253408.9:c.-22G>C	ENSP00000253408.4:n.-22G>C
ENST00000588957.5:c.-272+309G>C	ENSP00000465565.1:n.-272+309G>C
ENST00000593179.1:c.-22G>C	ENSP00000467106.1:n.-22G>C
NM_001131019.2:c.-22G>C	NP_001124491.1:n.-22G>C
NM_001242376.1:c.-22G>C	NP_001229305.1:n.-22G>C
NM_002055.4:c.-22G>C	NP_002046.1:n.-22G>C
NM_001363846.1:c.-22G>C	NP_001350775.1:n.-22G>C
XM_024450690.1:c.-22G>C	XP_024306458.1:n.-22G>C
XM_024450691.1:c.-22G>C	XP_024306459.1:n.-22G>C
XM_024450692.1:c.-22G>C	XP_024306460.1:n.-22G>C
XM_024450693.1:c.-22G>C	XP_024306461.1:n.-22G>C