Canonical Allele Identifier: CA8608935

Gene: GFAP

Linked Data

• dbSNP Id: rs144426492
• ExAC: 17:42991032 CTG / C
• gnomAD v2: 17-42991032-CTG-C
• gnomAD v3: 17-44913664-CTG-C
• gnomAD v4: 17-44913664-CTG-C
• MyVariant Identifiers: chr17:g.42991033_42991034del (hg19) ; chr17:g.44913665_44913666del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44913666_44913667del , CM000679.2:g.44913666_44913667del	GRCh38
NC_000017.10:g.42991034_42991035del , CM000679.1:g.42991034_42991035del	GRCh37
NC_000017.9:g.40346560_40346561del	NCBI36
NG_008401.1:g.6881_6882del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253408.11:c.618+62_618+63del	ENSP00000253408.5:n.618+62_618+63del
ENST00000435360.8:c.618+62_618+63del	ENSP00000403962.1:n.618+62_618+63del
ENST00000253408.10:c.618+62_618+63del	ENSP00000253408.5:n.618+62_618+63del
ENST00000435360.7:c.618+62_618+63del	ENSP00000403962.1:n.618+62_618+63del
ENST00000586127.6:n.1147+62_1147+63del
ENST00000586793.6:c.618+62_618+63del	ENSP00000468500.2:n.618+62_618+63del
ENST00000587997.6:n.31_32del
ENST00000588735.3:c.618+62_618+63del MANE Select	ENSP00000466598.2:n.618+62_618+63del
ENST00000591327.2:n.1772+62_1772+63del
ENST00000592320.6:c.618+62_618+63del	ENSP00000465320.1:n.618+62_618+63del
ENST00000638281.1:c.618+62_618+63del	ENSP00000491088.1:n.618+62_618+63del
ENST00000638618.1:c.273+62_273+63del	ENSP00000492832.1:n.273+62_273+63del
ENST00000639277.1:c.618+62_618+63del	ENSP00000492432.1:n.618+62_618+63del
ENST00000640552.1:n.632+62_632+63del
ENST00000253408.9:c.618+62_618+63del	ENSP00000253408.4:n.618+62_618+63del
ENST00000376990.8:c.*17+62_*17+63del	ENSP00000366189.4:n.*17+62_*17+63del
ENST00000435360.6:c.618+62_618+63del	ENSP00000403962.1:n.618+62_618+63del
ENST00000585728.5:c.*262+62_*262+63del	ENSP00000465208.1:n.*262+62_*262+63del
ENST00000586127.5:c.-44+62_-44+63del	ENSP00000464795.1:n.-44+62_-44+63del
ENST00000586793.5:c.618+62_618+63del	ENSP00000468500.1:n.618+62_618+63del
ENST00000587997.5:c.31_32del
ENST00000588316.1:c.523-236_523-235del	ENSP00000465629.1:n.523-236_523-235del
ENST00000588735.1:c.82+1739_82+1740del	ENSP00000466598.1:n.82+1739_82+1740del
ENST00000588957.5:c.-115+62_-115+63del	ENSP00000465565.1:n.-115+62_-115+63del
ENST00000590922.1:n.33_34del
ENST00000591327.1:n.571+62_571+63del
ENST00000592320.5:c.618+62_618+63del	ENSP00000465320.1:n.618+62_618+63del
NM_001131019.2:c.618+62_618+63del	NP_001124491.1:n.618+62_618+63del
NM_001242376.1:c.618+62_618+63del	NP_001229305.1:n.618+62_618+63del
NM_002055.4:c.618+62_618+63del	NP_002046.1:n.618+62_618+63del
NM_001363846.1:c.618+62_618+63del	NP_001350775.1:n.618+62_618+63del
XM_024450690.1:c.822+62_822+63del	XP_024306458.1:n.822+62_822+63del
XM_024450691.1:c.822+62_822+63del	XP_024306459.1:n.822+62_822+63del
XM_024450692.1:c.822+62_822+63del	XP_024306460.1:n.822+62_822+63del
XM_024450693.1:c.822+62_822+63del	XP_024306461.1:n.822+62_822+63del
NM_002055.5:c.618+62_618+63del MANE Select	NP_002046.1:n.618+62_618+63del
NM_001131019.3:c.618+62_618+63del	NP_001124491.1:n.618+62_618+63del
NM_001242376.2:c.618+62_618+63del	NP_001229305.1:n.618+62_618+63del
NM_001242376.3:c.618+62_618+63del	NP_001229305.1:n.618+62_618+63del
NM_001363846.2:c.618+62_618+63del	NP_001350775.1:n.618+62_618+63del