Canonical Allele Identifier: CA2638278250

Gene: GFAP

Linked Data

• gnomAD v4: 17-44915502-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44915502C>A , CM000679.2:g.44915502C>A	GRCh38
NC_000017.10:g.42992870C>A , CM000679.1:g.42992870C>A	GRCh37
NC_000017.9:g.40348396C>A	NCBI36
NG_008401.1:g.5045G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592320.6:c.-16G>T	ENSP00000465320.1:n.-16G>T
ENST00000253408.9:c.-16G>T	ENSP00000253408.4:n.-16G>T
ENST00000588037.1:c.-16G>T	ENSP00000466163.1:n.-16G>T
ENST00000588957.5:c.-272+315G>T	ENSP00000465565.1:n.-272+315G>T
ENST00000592320.5:c.-16G>T	ENSP00000465320.1:n.-16G>T
ENST00000593179.1:c.-16G>T	ENSP00000467106.1:n.-16G>T
NM_001131019.2:c.-16G>T	NP_001124491.1:n.-16G>T
NM_001242376.1:c.-16G>T	NP_001229305.1:n.-16G>T
NM_002055.4:c.-16G>T	NP_002046.1:n.-16G>T
NM_001363846.1:c.-16G>T	NP_001350775.1:n.-16G>T
XM_024450690.1:c.-16G>T	XP_024306458.1:n.-16G>T
XM_024450691.1:c.-16G>T	XP_024306459.1:n.-16G>T
XM_024450692.1:c.-16G>T	XP_024306460.1:n.-16G>T
XM_024450693.1:c.-16G>T	XP_024306461.1:n.-16G>T