Canonical Allele Identifier: CA2638273133
Gene: GFAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44907856G>A , CM000679.2:g.44907856G>A GRCh38
NC_000017.10:g.42985224G>A , CM000679.1:g.42985224G>A GRCh37
NC_000017.9:g.40340750G>A NCBI36
NG_008401.1:g.12691C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000253408.11:c.1377+208C>T ENSP00000253408.5:n.1377+208C>T
ENST00000253408.10:c.1377+208C>T ENSP00000253408.5:n.1377+208C>T
ENST00000441312.2:n.110+208C>T
ENST00000585543.6:n.410+208C>T
ENST00000586125.2:c.400C>T ENSP00000467397.2:n.400C>T
ENST00000588735.3:c.1257+208C>T MANE Select ENSP00000466598.2:n.1257+208C>T
ENST00000589701.2:n.2164+208C>T
ENST00000591880.2:c.564C>T
ENST00000592065.2:n.625+208C>T
ENST00000638304.1:c.176+208C>T
ENST00000638400.1:c.92+208C>T
ENST00000638488.1:n.721+208C>T
ENST00000638618.1:c.912+208C>T ENSP00000492832.1:n.912+208C>T
ENST00000638921.1:n.392C>T
ENST00000639042.1:c.229+208C>T
ENST00000639243.1:c.13+208C>T
ENST00000639277.1:c.1257+208C>T ENSP00000492432.1:n.1257+208C>T
ENST00000639369.1:c.107+208C>T
ENST00000640545.1:c.63+208C>T ENSP00000491735.1:n.63+208C>T
ENST00000640859.1:c.71+208C>T
ENST00000253408.9:c.1257+208C>T ENSP00000253408.4:n.1257+208C>T
ENST00000585543.5:n.410+208C>T
ENST00000588735.1:c.135+208C>T ENSP00000466598.1:n.135+208C>T
ENST00000589701.1:n.159+208C>T
ENST00000591880.1:c.331C>T ENSP00000467530.1:n.331C>T
ENST00000592065.1:n.51+208C>T
ENST00000592706.5:n.129+208C>T
NM_002055.4:c.1257+208C>T NP_002046.1:n.1257+208C>T
NM_001363846.1:c.1377+208C>T NP_001350775.1:n.1377+208C>T
XM_024450690.1:c.1581+208C>T XP_024306458.1:n.1581+208C>T
XM_024450692.1:c.1461+208C>T XP_024306460.1:n.1461+208C>T
NM_002055.5:c.1257+208C>T MANE Select NP_002046.1:n.1257+208C>T
NM_001363846.2:c.1377+208C>T NP_001350775.1:n.1377+208C>T