Canonical Allele Identifier: CA399845708

Gene: GFAP

Linked Data

• gnomAD v4: 17-44913336-A-C
• MyVariant Identifiers: chr17:g.42990704A>C (hg19) ; chr17:g.44913336A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44913336A>C , CM000679.2:g.44913336A>C	GRCh38
NC_000017.10:g.42990704A>C , CM000679.1:g.42990704A>C	GRCh37
NC_000017.9:g.40346230A>C	NCBI36
NG_008401.1:g.7211T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253408.11:c.713T>G	ENSP00000253408.5:p.Ile238Ser
ENST00000435360.8:c.713T>G	ENSP00000403962.1:p.Ile238Ser
ENST00000253408.10:c.713T>G	ENSP00000253408.5:p.Ile238Ser
ENST00000435360.7:c.713T>G	ENSP00000403962.1:p.Ile238Ser
ENST00000586127.6:n.1242T>G
ENST00000586793.6:c.713T>G	ENSP00000468500.2:p.Ile238Ser
ENST00000587997.6:n.189T>G
ENST00000588735.3:c.713T>G MANE Select	ENSP00000466598.2:p.Ile238Ser
ENST00000591327.2:n.1867T>G
ENST00000592320.6:c.618+392T>G	ENSP00000465320.1:n.618+392T>G
ENST00000638281.1:c.713T>G	ENSP00000491088.1:p.Ile238Ser
ENST00000638618.1:c.368T>G	ENSP00000492832.1:p.Ile123Ser
ENST00000639277.1:c.713T>G	ENSP00000492432.1:p.Ile238Ser
ENST00000640552.1:n.727T>G
ENST00000253408.9:c.713T>G	ENSP00000253408.4:p.Ile238Ser
ENST00000376990.8:c.*112T>G	ENSP00000366189.4:n.*112T>G
ENST00000435360.6:c.713T>G	ENSP00000403962.1:p.Ile238Ser
ENST00000585728.5:c.*357T>G	ENSP00000465208.1:n.*357T>G
ENST00000586793.5:c.713T>G	ENSP00000468500.1:p.Ile238Ser
ENST00000587997.5:c.189T>G
ENST00000588316.1:c.617T>G	ENSP00000465629.1:p.Ile206Ser
ENST00000588735.1:c.82+2069T>G	ENSP00000466598.1:n.82+2069T>G
ENST00000588957.5:c.-20T>G	ENSP00000465565.1:n.-20T>G
ENST00000590922.1:n.363T>G
ENST00000592320.5:c.618+392T>G	ENSP00000465320.1:n.618+392T>G
NM_001131019.2:c.713T>G	NP_001124491.1:p.Ile238Ser
NM_001242376.1:c.713T>G	NP_001229305.1:p.Ile238Ser
NM_002055.4:c.713T>G	NP_002046.1:p.Ile238Ser
NM_001363846.1:c.713T>G	NP_001350775.1:p.Ile238Ser
XM_024450690.1:c.917T>G	XP_024306458.1:p.Ile306Ser
XM_024450691.1:c.917T>G	XP_024306459.1:p.Ile306Ser
XM_024450692.1:c.917T>G	XP_024306460.1:p.Ile306Ser
XM_024450693.1:c.917T>G	XP_024306461.1:p.Ile306Ser
NM_002055.5:c.713T>G MANE Select	NP_002046.1:p.Ile238Ser
NM_001131019.3:c.713T>G	NP_001124491.1:p.Ile238Ser
NM_001242376.2:c.713T>G	NP_001229305.1:p.Ile238Ser
NM_001242376.3:c.713T>G	NP_001229305.1:p.Ile238Ser
NM_001363846.2:c.713T>G	NP_001350775.1:p.Ile238Ser