Canonical Allele Identifier: CA500321467
Gene: GFAP HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.42990673G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44913305G>A , CM000679.2:g.44913305G>A GRCh38
NC_000017.10:g.42990673G>A , CM000679.1:g.42990673G>A GRCh37
NC_000017.9:g.40346199G>A NCBI36
NG_008401.1:g.7242C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000253408.11:c.744C>T ENSP00000253408.5:p.Ser248=
ENST00000435360.8:c.744C>T ENSP00000403962.1:p.Ser248=
ENST00000253408.10:c.744C>T ENSP00000253408.5:p.Ser248=
ENST00000435360.7:c.744C>T ENSP00000403962.1:p.Ser248=
ENST00000586127.6:n.1273C>T
ENST00000586793.6:c.744C>T ENSP00000468500.2:p.Ser248=
ENST00000587997.6:n.220C>T
ENST00000588735.3:c.744C>T MANE Select ENSP00000466598.2:p.Ser248=
ENST00000591327.2:n.1898C>T
ENST00000592320.6:c.618+423C>T ENSP00000465320.1:n.618+423C>T
ENST00000638281.1:c.744C>T ENSP00000491088.1:p.Ser248=
ENST00000638618.1:c.399C>T ENSP00000492832.1:p.Ser133=
ENST00000639277.1:c.744C>T ENSP00000492432.1:p.Ser248=
ENST00000640552.1:n.758C>T
ENST00000253408.9:c.744C>T ENSP00000253408.4:p.Ser248=
ENST00000376990.8:c.*143C>T ENSP00000366189.4:n.*143C>T
ENST00000435360.6:c.744C>T ENSP00000403962.1:p.Ser248=
ENST00000586793.5:c.744C>T ENSP00000468500.1:p.Ser248=
ENST00000587997.5:c.220C>T
ENST00000588316.1:c.648C>T ENSP00000465629.1:p.Ser216=
ENST00000588735.1:c.82+2100C>T ENSP00000466598.1:n.82+2100C>T
ENST00000588957.5:c.12C>T ENSP00000465565.1:p.Ser4=
ENST00000590922.1:n.394C>T
ENST00000592320.5:c.618+423C>T ENSP00000465320.1:n.618+423C>T
NM_001131019.2:c.744C>T NP_001124491.1:p.Ser248=
NM_001242376.1:c.744C>T NP_001229305.1:p.Ser248=
NM_002055.4:c.744C>T NP_002046.1:p.Ser248=
NM_001363846.1:c.744C>T NP_001350775.1:p.Ser248=
XM_024450690.1:c.948C>T XP_024306458.1:p.Ser316=
XM_024450691.1:c.948C>T XP_024306459.1:p.Ser316=
XM_024450692.1:c.948C>T XP_024306460.1:p.Ser316=
XM_024450693.1:c.948C>T XP_024306461.1:p.Ser316=
NM_002055.5:c.744C>T MANE Select NP_002046.1:p.Ser248=
NM_001131019.3:c.744C>T NP_001124491.1:p.Ser248=
NM_001242376.2:c.744C>T NP_001229305.1:p.Ser248=
NM_001242376.3:c.744C>T NP_001229305.1:p.Ser248=
NM_001363846.2:c.744C>T NP_001350775.1:p.Ser248=