Canonical Allele Identifier: CA399848618

Gene: GFAP

Linked Data

• ClinVar Variation Id: 432046
• ClinVar RCV Id: RCV000498900 ; RCV002051858
• dbSNP Id: rs571151302
• MyVariant Identifiers: chr17:g.42992603G>C (hg19) ; chr17:g.44915235G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44915235G>C , CM000679.2:g.44915235G>C	GRCh38
NC_000017.10:g.42992603G>C , CM000679.1:g.42992603G>C	GRCh37
NC_000017.9:g.40348129G>C	NCBI36
NG_008401.1:g.5312C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253408.11:c.252C>G	ENSP00000253408.5:p.Ile84Met
ENST00000435360.8:c.252C>G	ENSP00000403962.1:p.Ile84Met
ENST00000253408.10:c.252C>G	ENSP00000253408.5:p.Ile84Met
ENST00000435360.7:c.252C>G	ENSP00000403962.1:p.Ile84Met
ENST00000586793.6:c.252C>G	ENSP00000468500.2:p.Ile84Met
ENST00000588735.3:c.252C>G MANE Select	ENSP00000466598.2:p.Ile84Met
ENST00000591327.2:n.265C>G
ENST00000592320.6:c.252C>G	ENSP00000465320.1:p.Ile84Met
ENST00000638281.1:c.252C>G	ENSP00000491088.1:p.Ile84Met
ENST00000639277.1:c.252C>G	ENSP00000492432.1:p.Ile84Met
ENST00000640552.1:n.266C>G
ENST00000253408.9:c.252C>G	ENSP00000253408.4:p.Ile84Met
ENST00000376990.8:c.252C>G	ENSP00000366189.4:p.Ile84Met
ENST00000435360.6:c.252C>G	ENSP00000403962.1:p.Ile84Met
ENST00000585728.5:c.181+71C>G	ENSP00000465208.1:n.181+71C>G
ENST00000586793.5:c.252C>G	ENSP00000468500.1:p.Ile84Met
ENST00000588037.1:c.252C>G	ENSP00000466163.1:p.Ile84Met
ENST00000588316.1:c.252C>G	ENSP00000465629.1:p.Ile84Met
ENST00000588735.1:c.82+170C>G	ENSP00000466598.1:n.82+170C>G
ENST00000588957.5:c.-272+582C>G	ENSP00000465565.1:n.-272+582C>G
ENST00000591327.1:n.266C>G
ENST00000592320.5:c.252C>G	ENSP00000465320.1:p.Ile84Met
NM_001131019.2:c.252C>G	NP_001124491.1:p.Ile84Met
NM_001242376.1:c.252C>G	NP_001229305.1:p.Ile84Met
NM_002055.4:c.252C>G	NP_002046.1:p.Ile84Met
NM_001363846.1:c.252C>G	NP_001350775.1:p.Ile84Met
XM_024450690.1:c.252C>G	XP_024306458.1:p.Ile84Met
XM_024450691.1:c.252C>G	XP_024306459.1:p.Ile84Met
XM_024450692.1:c.252C>G	XP_024306460.1:p.Ile84Met
XM_024450693.1:c.252C>G	XP_024306461.1:p.Ile84Met
NM_002055.5:c.252C>G MANE Select	NP_002046.1:p.Ile84Met
NM_001131019.3:c.252C>G	NP_001124491.1:p.Ile84Met
NM_001242376.2:c.252C>G	NP_001229305.1:p.Ile84Met
NM_001242376.3:c.252C>G	NP_001229305.1:p.Ile84Met
NM_001363846.2:c.252C>G	NP_001350775.1:p.Ile84Met