Canonical Allele Identifier: CA291024337

Gene: GFAP

Linked Data

• dbSNP Id: rs115319963
• gnomAD v2: 17-42985189-G-C
• gnomAD v3: 17-44907821-G-C
• gnomAD v4: 17-44907821-G-C
• MyVariant Identifiers: chr17:g.42985189G>C (hg19) ; chr17:g.44907821G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44907821G>C , CM000679.2:g.44907821G>C	GRCh38
NC_000017.10:g.42985189G>C , CM000679.1:g.42985189G>C	GRCh37
NC_000017.9:g.40340715G>C	NCBI36
NG_008401.1:g.12726C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253408.11:c.1377+243C>G	ENSP00000253408.5:n.1377+243C>G
ENST00000253408.10:c.1377+243C>G	ENSP00000253408.5:n.1377+243C>G
ENST00000441312.2:n.110+243C>G
ENST00000585543.6:n.410+243C>G
ENST00000586125.2:c.435C>G	ENSP00000467397.2:n.435C>G
ENST00000588735.3:c.1257+243C>G MANE Select	ENSP00000466598.2:n.1257+243C>G
ENST00000589701.2:n.2164+243C>G
ENST00000591880.2:c.599C>G
ENST00000592065.2:n.625+243C>G
ENST00000638304.1:c.176+243C>G
ENST00000638400.1:c.92+243C>G
ENST00000638488.1:n.721+243C>G
ENST00000638618.1:c.912+243C>G	ENSP00000492832.1:n.912+243C>G
ENST00000638921.1:n.427C>G
ENST00000639042.1:c.229+243C>G
ENST00000639243.1:c.13+243C>G
ENST00000639277.1:c.1257+243C>G	ENSP00000492432.1:n.1257+243C>G
ENST00000639369.1:c.107+243C>G
ENST00000640545.1:c.63+243C>G	ENSP00000491735.1:n.63+243C>G
ENST00000640859.1:c.71+243C>G
ENST00000253408.9:c.1257+243C>G	ENSP00000253408.4:n.1257+243C>G
ENST00000585543.5:n.410+243C>G
ENST00000588735.1:c.135+243C>G	ENSP00000466598.1:n.135+243C>G
ENST00000589701.1:n.159+243C>G
ENST00000591880.1:c.366C>G	ENSP00000467530.1:n.366C>G
ENST00000592065.1:n.51+243C>G
ENST00000592706.5:n.129+243C>G
NM_002055.4:c.1257+243C>G	NP_002046.1:n.1257+243C>G
NM_001363846.1:c.1377+243C>G	NP_001350775.1:n.1377+243C>G
XM_024450690.1:c.1581+243C>G	XP_024306458.1:n.1581+243C>G
XM_024450692.1:c.1461+243C>G	XP_024306460.1:n.1461+243C>G
NM_002055.5:c.1257+243C>G MANE Select	NP_002046.1:n.1257+243C>G
NM_001363846.2:c.1377+243C>G	NP_001350775.1:n.1377+243C>G