Canonical Allele Identifier: CA2638262717

Gene: GFAP

Linked Data

• gnomAD v4: 17-44908284-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44908284A>G , CM000679.2:g.44908284A>G	GRCh38
NC_000017.10:g.42985652A>G , CM000679.1:g.42985652A>G	GRCh37
NC_000017.9:g.40341178A>G	NCBI36
NG_008401.1:g.12263T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253408.11:c.1292-135T>C	ENSP00000253408.5:n.1292-135T>C
ENST00000253408.10:c.1292-135T>C	ENSP00000253408.5:n.1292-135T>C
ENST00000441312.2:n.25-135T>C
ENST00000585543.6:n.325-135T>C
ENST00000586125.2:c.107-135T>C	ENSP00000467397.2:n.107-135T>C
ENST00000588735.3:c.1172-135T>C MANE Select	ENSP00000466598.2:n.1172-135T>C
ENST00000589701.2:n.1944T>C
ENST00000591880.2:c.271-135T>C
ENST00000592065.2:n.405T>C
ENST00000638304.1:c.91-135T>C
ENST00000638400.1:c.7-135T>C
ENST00000638488.1:n.636-135T>C
ENST00000638618.1:c.827-135T>C	ENSP00000492832.1:n.827-135T>C
ENST00000639042.1:c.144-135T>C
ENST00000639277.1:c.1172-135T>C	ENSP00000492432.1:n.1172-135T>C
ENST00000639369.1:c.22-135T>C
ENST00000640552.1:n.3516T>C
ENST00000253408.9:c.1172-135T>C	ENSP00000253408.4:n.1172-135T>C
ENST00000585543.5:n.325-135T>C
ENST00000586125.1:c.143-135T>C	ENSP00000467397.1:n.143-135T>C
ENST00000588640.5:n.552-135T>C
ENST00000588735.1:c.83-168T>C	ENSP00000466598.1:n.83-168T>C
ENST00000591880.1:c.38-135T>C	ENSP00000467530.1:n.38-135T>C
ENST00000592706.5:n.44-135T>C
NM_002055.4:c.1172-135T>C	NP_002046.1:n.1172-135T>C
NM_001363846.1:c.1292-135T>C	NP_001350775.1:n.1292-135T>C
XM_024450690.1:c.1496-135T>C	XP_024306458.1:n.1496-135T>C
XM_024450692.1:c.1376-135T>C	XP_024306460.1:n.1376-135T>C
NM_002055.5:c.1172-135T>C MANE Select	NP_002046.1:n.1172-135T>C
NM_001242376.2:c.*2185T>C	NP_001229305.1:n.*2185T>C
NM_001363846.2:c.1292-135T>C	NP_001350775.1:n.1292-135T>C