Canonical Allele Identifier: CA2638262604

Gene: GFAP

Linked Data

• gnomAD v4: 17-44908267-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44908267C>A , CM000679.2:g.44908267C>A	GRCh38
NC_000017.10:g.42985635C>A , CM000679.1:g.42985635C>A	GRCh37
NC_000017.9:g.40341161C>A	NCBI36
NG_008401.1:g.12280G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253408.11:c.1292-118G>T	ENSP00000253408.5:n.1292-118G>T
ENST00000253408.10:c.1292-118G>T	ENSP00000253408.5:n.1292-118G>T
ENST00000441312.2:n.25-118G>T
ENST00000585543.6:n.325-118G>T
ENST00000586125.2:c.107-118G>T	ENSP00000467397.2:n.107-118G>T
ENST00000588735.3:c.1172-118G>T MANE Select	ENSP00000466598.2:n.1172-118G>T
ENST00000589701.2:n.1961G>T
ENST00000591880.2:c.271-118G>T
ENST00000592065.2:n.422G>T
ENST00000638304.1:c.91-118G>T
ENST00000638400.1:c.7-118G>T
ENST00000638488.1:n.636-118G>T
ENST00000638618.1:c.827-118G>T	ENSP00000492832.1:n.827-118G>T
ENST00000639042.1:c.144-118G>T
ENST00000639277.1:c.1172-118G>T	ENSP00000492432.1:n.1172-118G>T
ENST00000639369.1:c.22-118G>T
ENST00000640552.1:n.3533G>T
ENST00000253408.9:c.1172-118G>T	ENSP00000253408.4:n.1172-118G>T
ENST00000585543.5:n.325-118G>T
ENST00000586125.1:c.143-118G>T	ENSP00000467397.1:n.143-118G>T
ENST00000588640.5:n.552-118G>T
ENST00000588735.1:c.83-151G>T	ENSP00000466598.1:n.83-151G>T
ENST00000591880.1:c.38-118G>T	ENSP00000467530.1:n.38-118G>T
ENST00000592706.5:n.44-118G>T
NM_002055.4:c.1172-118G>T	NP_002046.1:n.1172-118G>T
NM_001363846.1:c.1292-118G>T	NP_001350775.1:n.1292-118G>T
XM_024450690.1:c.1496-118G>T	XP_024306458.1:n.1496-118G>T
XM_024450692.1:c.1376-118G>T	XP_024306460.1:n.1376-118G>T
NM_002055.5:c.1172-118G>T MANE Select	NP_002046.1:n.1172-118G>T
NM_001242376.2:c.*2202G>T	NP_001229305.1:n.*2202G>T
NM_001363846.2:c.1292-118G>T	NP_001350775.1:n.1292-118G>T