Canonical Allele Identifier: CA399845443
Gene: GFAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44913278G>T , CM000679.2:g.44913278G>T GRCh38
NC_000017.10:g.42990646G>T , CM000679.1:g.42990646G>T GRCh37
NC_000017.9:g.40346172G>T NCBI36
NG_008401.1:g.7269C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000253408.11:c.771C>A ENSP00000253408.5:p.Tyr257Ter
ENST00000435360.8:c.771C>A ENSP00000403962.1:p.Tyr257Ter
ENST00000253408.10:c.771C>A ENSP00000253408.5:p.Tyr257Ter
ENST00000435360.7:c.771C>A ENSP00000403962.1:p.Tyr257Ter
ENST00000586127.6:n.1300C>A
ENST00000586793.6:c.771C>A ENSP00000468500.2:p.Tyr257Ter
ENST00000587997.6:n.247C>A
ENST00000588735.3:c.771C>A MANE Select ENSP00000466598.2:p.Tyr257Ter
ENST00000591327.2:n.1925C>A
ENST00000592320.6:c.618+450C>A ENSP00000465320.1:n.618+450C>A
ENST00000638281.1:c.771C>A ENSP00000491088.1:p.Tyr257Ter
ENST00000638618.1:c.426C>A ENSP00000492832.1:p.Tyr142Ter
ENST00000639277.1:c.771C>A ENSP00000492432.1:p.Tyr257Ter
ENST00000640552.1:n.785C>A
ENST00000253408.9:c.771C>A ENSP00000253408.4:p.Tyr257Ter
ENST00000376990.8:c.*170C>A ENSP00000366189.4:n.*170C>A
ENST00000435360.6:c.771C>A ENSP00000403962.1:p.Tyr257Ter
ENST00000586793.5:c.771C>A ENSP00000468500.1:p.Tyr257Ter
ENST00000587997.5:c.247C>A
ENST00000588316.1:c.675C>A ENSP00000465629.1:p.Tyr225Ter
ENST00000588735.1:c.82+2127C>A ENSP00000466598.1:n.82+2127C>A
ENST00000588957.5:c.39C>A ENSP00000465565.1:p.Tyr13Ter
ENST00000590922.1:n.421C>A
ENST00000592320.5:c.618+450C>A ENSP00000465320.1:n.618+450C>A
NM_001131019.2:c.771C>A NP_001124491.1:p.Tyr257Ter
NM_001242376.1:c.771C>A NP_001229305.1:p.Tyr257Ter
NM_002055.4:c.771C>A NP_002046.1:p.Tyr257Ter
NM_001363846.1:c.771C>A NP_001350775.1:p.Tyr257Ter
XM_024450690.1:c.975C>A XP_024306458.1:p.Tyr325Ter
XM_024450691.1:c.975C>A XP_024306459.1:p.Tyr325Ter
XM_024450692.1:c.975C>A XP_024306460.1:p.Tyr325Ter
XM_024450693.1:c.975C>A XP_024306461.1:p.Tyr325Ter
NM_002055.5:c.771C>A MANE Select NP_002046.1:p.Tyr257Ter
NM_001131019.3:c.771C>A NP_001124491.1:p.Tyr257Ter
NM_001242376.2:c.771C>A NP_001229305.1:p.Tyr257Ter
NM_001242376.3:c.771C>A NP_001229305.1:p.Tyr257Ter
NM_001363846.2:c.771C>A NP_001350775.1:p.Tyr257Ter