Canonical Allele Identifier: CA399838119

Gene: GFAP

Linked Data

• gnomAD v4: 17-44907942-T-G
• MyVariant Identifiers: chr17:g.42985310T>G (hg19) ; chr17:g.44907942T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44907942T>G , CM000679.2:g.44907942T>G	GRCh38
NC_000017.10:g.42985310T>G , CM000679.1:g.42985310T>G	GRCh37
NC_000017.9:g.40340836T>G	NCBI36
NG_008401.1:g.12605A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253408.11:c.1377+122A>C	ENSP00000253408.5:n.1377+122A>C
ENST00000253408.10:c.1377+122A>C	ENSP00000253408.5:n.1377+122A>C
ENST00000441312.2:n.110+122A>C
ENST00000585543.6:n.410+122A>C
ENST00000586125.2:c.314A>C	ENSP00000467397.2:p.Gln105Pro
ENST00000588735.3:c.1257+122A>C MANE Select	ENSP00000466598.2:n.1257+122A>C
ENST00000589701.2:n.2164+122A>C
ENST00000591880.2:c.478A>C
ENST00000592065.2:n.625+122A>C
ENST00000638304.1:c.176+122A>C
ENST00000638400.1:c.92+122A>C
ENST00000638488.1:n.721+122A>C
ENST00000638618.1:c.912+122A>C	ENSP00000492832.1:n.912+122A>C
ENST00000638921.1:n.306A>C
ENST00000639042.1:c.229+122A>C
ENST00000639243.1:c.13+122A>C
ENST00000639277.1:c.1257+122A>C	ENSP00000492432.1:n.1257+122A>C
ENST00000639369.1:c.107+122A>C
ENST00000640545.1:c.63+122A>C	ENSP00000491735.1:n.63+122A>C
ENST00000640859.1:c.71+122A>C
ENST00000253408.9:c.1257+122A>C	ENSP00000253408.4:n.1257+122A>C
ENST00000585543.5:n.410+122A>C
ENST00000588735.1:c.135+122A>C	ENSP00000466598.1:n.135+122A>C
ENST00000589701.1:n.159+122A>C
ENST00000591880.1:c.245A>C	ENSP00000467530.1:p.Gln82Pro
ENST00000592065.1:n.51+122A>C
ENST00000592706.5:n.129+122A>C
NM_002055.4:c.1257+122A>C	NP_002046.1:n.1257+122A>C
NM_001363846.1:c.1377+122A>C	NP_001350775.1:n.1377+122A>C
XM_024450690.1:c.1581+122A>C	XP_024306458.1:n.1581+122A>C
XM_024450692.1:c.1461+122A>C	XP_024306460.1:n.1461+122A>C
NM_002055.5:c.1257+122A>C MANE Select	NP_002046.1:n.1257+122A>C
NM_001363846.2:c.1377+122A>C	NP_001350775.1:n.1377+122A>C