Canonical Allele Identifier: CA291034768

Gene: GFAP

Linked Data

• dbSNP Id: rs113095913
• MyVariant Identifiers: chr17:g.42992869G>C (hg19) ; chr17:g.44915501G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44915501G>C , CM000679.2:g.44915501G>C	GRCh38
NC_000017.10:g.42992869G>C , CM000679.1:g.42992869G>C	GRCh37
NC_000017.9:g.40348395G>C	NCBI36
NG_008401.1:g.5046C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592320.6:c.-15C>G	ENSP00000465320.1:n.-15C>G
ENST00000253408.9:c.-15C>G	ENSP00000253408.4:n.-15C>G
ENST00000588037.1:c.-15C>G	ENSP00000466163.1:n.-15C>G
ENST00000588957.5:c.-272+316C>G	ENSP00000465565.1:n.-272+316C>G
ENST00000592320.5:c.-15C>G	ENSP00000465320.1:n.-15C>G
ENST00000593179.1:c.-15C>G	ENSP00000467106.1:n.-15C>G
NM_001131019.2:c.-15C>G	NP_001124491.1:n.-15C>G
NM_001242376.1:c.-15C>G	NP_001229305.1:n.-15C>G
NM_002055.4:c.-15C>G	NP_002046.1:n.-15C>G
NM_001363846.1:c.-15C>G	NP_001350775.1:n.-15C>G
XM_024450690.1:c.-15C>G	XP_024306458.1:n.-15C>G
XM_024450691.1:c.-15C>G	XP_024306459.1:n.-15C>G
XM_024450692.1:c.-15C>G	XP_024306460.1:n.-15C>G
XM_024450693.1:c.-15C>G	XP_024306461.1:n.-15C>G