Canonical Allele Identifier: CA2638272822
Gene: GFAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44911197_44911262dup , CM000679.2:g.44911197_44911262dup GRCh38
NC_000017.10:g.42988565_42988630dup , CM000679.1:g.42988565_42988630dup GRCh37
NC_000017.9:g.40344091_40344156dup NCBI36
NG_008401.1:g.9286_9351dup

Transcript Alleles

HGVS Amino-acid change
ENST00000253408.11:c.1102_1127+40dup
ENST00000435360.8:c.1102_1127+40dup
ENST00000253408.10:c.1102_1127+40dup
ENST00000435360.7:c.1102_1127+40dup
ENST00000585543.6:n.255_280+40dup
ENST00000586125.2:c.37_62+40dup
ENST00000586127.6:n.1631_1656+40dup
ENST00000586793.6:c.967_992+40dup
ENST00000587997.6:n.578_603+40dup
ENST00000588735.3:c.1102_1127+40dup
ENST00000591327.2:n.2256_2281+40dup
ENST00000591880.2:c.32_57+40dup
ENST00000592320.6:c.679_704+40dup
ENST00000638281.1:c.1102_1127+40dup
ENST00000638304.1:c.21_46+40dup
ENST00000638488.1:n.43_68+40dup
ENST00000638618.1:c.757_782+40dup
ENST00000639042.1:c.39_64+40dup
ENST00000639277.1:c.1102_1127+40dup
ENST00000639921.1:c.59_84+40dup
ENST00000640552.1:n.1116_1141+40dup
ENST00000253408.9:c.1102_1127+40dup
ENST00000435360.6:c.1102_1127+40dup
ENST00000585543.5:n.255_280+40dup
ENST00000586793.5:c.1102_1127+40dup
ENST00000588640.5:n.482_507+40dup
ENST00000588735.1:c.83-3145_83-3080dup ENSP00000466598.1:n.83-3145_83-3080dup
ENST00000592320.5:c.679_704+40dup
NM_001131019.2:c.1102_1127+40dup
NM_001242376.1:c.1102_1127+40dup
NM_002055.4:c.1102_1127+40dup
NM_001363846.1:c.1102_1127+40dup
XM_024450690.1:c.1306_1331+40dup
XM_024450691.1:c.1306_1331+40dup
XM_024450692.1:c.1306_1331+40dup
XM_024450693.1:c.1306_1331+40dup
NM_002055.5:c.1102_1127+40dup
NM_001131019.3:c.1102_1127+40dup
NM_001242376.2:c.1102_1127+40dup
NM_001242376.3:c.1102_1127+40dup
NM_001363846.2:c.1102_1127+40dup