Canonical Allele Identifier: CA2638278256

Gene: GFAP

Linked Data

• gnomAD v4: 17-44915507-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44915507T>C , CM000679.2:g.44915507T>C	GRCh38
NC_000017.10:g.42992875T>C , CM000679.1:g.42992875T>C	GRCh37
NC_000017.9:g.40348401T>C	NCBI36
NG_008401.1:g.5040A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253408.9:c.-21A>G	ENSP00000253408.4:n.-21A>G
ENST00000588957.5:c.-272+310A>G	ENSP00000465565.1:n.-272+310A>G
ENST00000593179.1:c.-21A>G	ENSP00000467106.1:n.-21A>G
NM_001131019.2:c.-21A>G	NP_001124491.1:n.-21A>G
NM_001242376.1:c.-21A>G	NP_001229305.1:n.-21A>G
NM_002055.4:c.-21A>G	NP_002046.1:n.-21A>G
NM_001363846.1:c.-21A>G	NP_001350775.1:n.-21A>G
XM_024450690.1:c.-21A>G	XP_024306458.1:n.-21A>G
XM_024450691.1:c.-21A>G	XP_024306459.1:n.-21A>G
XM_024450692.1:c.-21A>G	XP_024306460.1:n.-21A>G
XM_024450693.1:c.-21A>G	XP_024306461.1:n.-21A>G