Canonical Allele Identifier: CA772333348

Gene: GFAP

Linked Data

• dbSNP Id: rs1323364345
• gnomAD v4: 17-44912871-G-T
• MyVariant Identifiers: chr17:g.42990239G>T (hg19) ; chr17:g.44912871G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44912871G>T , CM000679.2:g.44912871G>T	GRCh38
NC_000017.10:g.42990239G>T , CM000679.1:g.42990239G>T	GRCh37
NC_000017.9:g.40345765G>T	NCBI36
NG_008401.1:g.7676C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253408.11:c.780+398C>A	ENSP00000253408.5:n.780+398C>A
ENST00000435360.8:c.780+398C>A	ENSP00000403962.1:n.780+398C>A
ENST00000253408.10:c.780+398C>A	ENSP00000253408.5:n.780+398C>A
ENST00000435360.7:c.780+398C>A	ENSP00000403962.1:n.780+398C>A
ENST00000586127.6:n.1309+398C>A
ENST00000586793.6:c.780+398C>A	ENSP00000468500.2:n.780+398C>A
ENST00000587997.6:n.256+398C>A
ENST00000588735.3:c.780+398C>A MANE Select	ENSP00000466598.2:n.780+398C>A
ENST00000591327.2:n.1934+398C>A
ENST00000592320.6:c.618+857C>A	ENSP00000465320.1:n.618+857C>A
ENST00000638281.1:c.780+398C>A	ENSP00000491088.1:n.780+398C>A
ENST00000638618.1:c.435+398C>A	ENSP00000492832.1:n.435+398C>A
ENST00000639277.1:c.780+398C>A	ENSP00000492432.1:n.780+398C>A
ENST00000640552.1:n.794+398C>A
ENST00000253408.9:c.780+398C>A	ENSP00000253408.4:n.780+398C>A
ENST00000376990.8:c.*179+398C>A	ENSP00000366189.4:n.*179+398C>A
ENST00000435360.6:c.780+398C>A	ENSP00000403962.1:n.780+398C>A
ENST00000586793.5:c.780+398C>A	ENSP00000468500.1:n.780+398C>A
ENST00000587997.5:c.256+398C>A
ENST00000588316.1:c.684+398C>A	ENSP00000465629.1:n.684+398C>A
ENST00000588640.5:n.64C>A
ENST00000588735.1:c.82+2534C>A	ENSP00000466598.1:n.82+2534C>A
ENST00000588957.5:c.48+398C>A	ENSP00000465565.1:n.48+398C>A
ENST00000590922.1:n.430+398C>A
ENST00000592320.5:c.618+857C>A	ENSP00000465320.1:n.618+857C>A
NM_001131019.2:c.780+398C>A	NP_001124491.1:n.780+398C>A
NM_001242376.1:c.780+398C>A	NP_001229305.1:n.780+398C>A
NM_002055.4:c.780+398C>A	NP_002046.1:n.780+398C>A
NM_001363846.1:c.780+398C>A	NP_001350775.1:n.780+398C>A
XM_024450690.1:c.984+398C>A	XP_024306458.1:n.984+398C>A
XM_024450691.1:c.984+398C>A	XP_024306459.1:n.984+398C>A
XM_024450692.1:c.984+398C>A	XP_024306460.1:n.984+398C>A
XM_024450693.1:c.984+398C>A	XP_024306461.1:n.984+398C>A
NM_002055.5:c.780+398C>A MANE Select	NP_002046.1:n.780+398C>A
NM_001131019.3:c.780+398C>A	NP_001124491.1:n.780+398C>A
NM_001242376.2:c.780+398C>A	NP_001229305.1:n.780+398C>A
NM_001242376.3:c.780+398C>A	NP_001229305.1:n.780+398C>A
NM_001363846.2:c.780+398C>A	NP_001350775.1:n.780+398C>A