Canonical Allele Identifier: CA2576294661

Gene: GFAP

Linked Data

• gnomAD v4: 17-44915527-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44915527A>G , CM000679.2:g.44915527A>G	GRCh38
NC_000017.10:g.42992895A>G , CM000679.1:g.42992895A>G	GRCh37
NC_000017.9:g.40348421A>G	NCBI36
NG_008401.1:g.5020T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253408.9:c.-41T>C	ENSP00000253408.4:n.-41T>C
ENST00000588957.5:c.-272+290T>C	ENSP00000465565.1:n.-272+290T>C
ENST00000593179.1:c.-22-19T>C	ENSP00000467106.1:n.-22-19T>C
NM_001131019.2:c.-41T>C	NP_001124491.1:n.-41T>C
NM_001242376.1:c.-41T>C	NP_001229305.1:n.-41T>C
NM_002055.4:c.-41T>C	NP_002046.1:n.-41T>C
NM_001363846.1:c.-41T>C	NP_001350775.1:n.-41T>C
XM_024450690.1:c.-41T>C	XP_024306458.1:n.-41T>C
XM_024450691.1:c.-41T>C	XP_024306459.1:n.-41T>C
XM_024450692.1:c.-41T>C	XP_024306460.1:n.-41T>C
XM_024450693.1:c.-41T>C	XP_024306461.1:n.-41T>C