Canonical Allele Identifier: CA399845596

Gene: GFAP

Linked Data

• MyVariant Identifiers: chr17:g.42990669T>C (hg19) ; chr17:g.44913301T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44913301T>C , CM000679.2:g.44913301T>C	GRCh38
NC_000017.10:g.42990669T>C , CM000679.1:g.42990669T>C	GRCh37
NC_000017.9:g.40346195T>C	NCBI36
NG_008401.1:g.7246A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253408.11:c.748A>G	ENSP00000253408.5:p.Met250Val
ENST00000435360.8:c.748A>G	ENSP00000403962.1:p.Met250Val
ENST00000253408.10:c.748A>G	ENSP00000253408.5:p.Met250Val
ENST00000435360.7:c.748A>G	ENSP00000403962.1:p.Met250Val
ENST00000586127.6:n.1277A>G
ENST00000586793.6:c.748A>G	ENSP00000468500.2:p.Met250Val
ENST00000587997.6:n.224A>G
ENST00000588735.3:c.748A>G MANE Select	ENSP00000466598.2:p.Met250Val
ENST00000591327.2:n.1902A>G
ENST00000592320.6:c.618+427A>G	ENSP00000465320.1:n.618+427A>G
ENST00000638281.1:c.748A>G	ENSP00000491088.1:p.Met250Val
ENST00000638618.1:c.403A>G	ENSP00000492832.1:p.Met135Val
ENST00000639277.1:c.748A>G	ENSP00000492432.1:p.Met250Val
ENST00000640552.1:n.762A>G
ENST00000253408.9:c.748A>G	ENSP00000253408.4:p.Met250Val
ENST00000376990.8:c.*147A>G	ENSP00000366189.4:n.*147A>G
ENST00000435360.6:c.748A>G	ENSP00000403962.1:p.Met250Val
ENST00000586793.5:c.748A>G	ENSP00000468500.1:p.Met250Val
ENST00000587997.5:c.224A>G
ENST00000588316.1:c.652A>G	ENSP00000465629.1:p.Met218Val
ENST00000588735.1:c.82+2104A>G	ENSP00000466598.1:n.82+2104A>G
ENST00000588957.5:c.16A>G	ENSP00000465565.1:p.Met6Val
ENST00000590922.1:n.398A>G
ENST00000592320.5:c.618+427A>G	ENSP00000465320.1:n.618+427A>G
NM_001131019.2:c.748A>G	NP_001124491.1:p.Met250Val
NM_001242376.1:c.748A>G	NP_001229305.1:p.Met250Val
NM_002055.4:c.748A>G	NP_002046.1:p.Met250Val
NM_001363846.1:c.748A>G	NP_001350775.1:p.Met250Val
XM_024450690.1:c.952A>G	XP_024306458.1:p.Met318Val
XM_024450691.1:c.952A>G	XP_024306459.1:p.Met318Val
XM_024450692.1:c.952A>G	XP_024306460.1:p.Met318Val
XM_024450693.1:c.952A>G	XP_024306461.1:p.Met318Val
NM_002055.5:c.748A>G MANE Select	NP_002046.1:p.Met250Val
NM_001131019.3:c.748A>G	NP_001124491.1:p.Met250Val
NM_001242376.2:c.748A>G	NP_001229305.1:p.Met250Val
NM_001242376.3:c.748A>G	NP_001229305.1:p.Met250Val
NM_001363846.2:c.748A>G	NP_001350775.1:p.Met250Val