Canonical Allele Identifier: CA2638261785

Gene: GFAP

Linked Data

• gnomAD v4: 17-44908168-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44908168G>T , CM000679.2:g.44908168G>T	GRCh38
NC_000017.10:g.42985536G>T , CM000679.1:g.42985536G>T	GRCh37
NC_000017.9:g.40341062G>T	NCBI36
NG_008401.1:g.12379C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253408.11:c.1292-19C>A	ENSP00000253408.5:n.1292-19C>A
ENST00000253408.10:c.1292-19C>A	ENSP00000253408.5:n.1292-19C>A
ENST00000441312.2:n.25-19C>A
ENST00000585543.6:n.325-19C>A
ENST00000586125.2:c.107-19C>A	ENSP00000467397.2:n.107-19C>A
ENST00000588735.3:c.1172-19C>A MANE Select	ENSP00000466598.2:n.1172-19C>A
ENST00000589701.2:n.2060C>A
ENST00000591880.2:c.271-19C>A
ENST00000592065.2:n.521C>A
ENST00000638304.1:c.91-19C>A
ENST00000638400.1:c.7-19C>A
ENST00000638488.1:n.636-19C>A
ENST00000638618.1:c.827-19C>A	ENSP00000492832.1:n.827-19C>A
ENST00000638921.1:n.80C>A
ENST00000639042.1:c.144-19C>A
ENST00000639277.1:c.1172-19C>A	ENSP00000492432.1:n.1172-19C>A
ENST00000639369.1:c.22-19C>A
ENST00000253408.9:c.1172-19C>A	ENSP00000253408.4:n.1172-19C>A
ENST00000585543.5:n.325-19C>A
ENST00000586125.1:c.143-19C>A	ENSP00000467397.1:n.143-19C>A
ENST00000588640.5:n.552-19C>A
ENST00000588735.1:c.83-52C>A	ENSP00000466598.1:n.83-52C>A
ENST00000589701.1:n.55C>A
ENST00000591880.1:c.38-19C>A	ENSP00000467530.1:n.38-19C>A
ENST00000592706.5:n.44-19C>A
NM_002055.4:c.1172-19C>A	NP_002046.1:n.1172-19C>A
NM_001363846.1:c.1292-19C>A	NP_001350775.1:n.1292-19C>A
XM_024450690.1:c.1496-19C>A	XP_024306458.1:n.1496-19C>A
XM_024450692.1:c.1376-19C>A	XP_024306460.1:n.1376-19C>A
NM_002055.5:c.1172-19C>A MANE Select	NP_002046.1:n.1172-19C>A
NM_001363846.2:c.1292-19C>A	NP_001350775.1:n.1292-19C>A