Canonical Allele Identifier: CA2261612500

Gene: GFAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44912979_44912980delinsCA , CM000679.2:g.44912979_44912980delinsCA	GRCh38
NC_000017.10:g.42990347_42990348delinsCA , CM000679.1:g.42990347_42990348delinsCA	GRCh37
NC_000017.9:g.40345873_40345874delinsCA	NCBI36
NG_008401.1:g.7567_7568delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253408.11:c.780+289_780+290delinsTG	ENSP00000253408.5:n.780+289_780+290delinsTG
ENST00000435360.8:c.780+289_780+290delinsTG	ENSP00000403962.1:n.780+289_780+290delinsTG
ENST00000253408.10:c.780+289_780+290delinsTG	ENSP00000253408.5:n.780+289_780+290delinsTG
ENST00000435360.7:c.780+289_780+290delinsTG	ENSP00000403962.1:n.780+289_780+290delinsTG
ENST00000586127.6:n.1309+289_1309+290delinsTG
ENST00000586793.6:c.780+289_780+290delinsTG	ENSP00000468500.2:n.780+289_780+290delinsTG
ENST00000587997.6:n.256+289_256+290delinsTG
ENST00000588735.3:c.780+289_780+290delinsTG MANE Select	ENSP00000466598.2:n.780+289_780+290delinsTG
ENST00000591327.2:n.1934+289_1934+290delinsTG
ENST00000592320.6:c.618+748_618+749delinsTG	ENSP00000465320.1:n.618+748_618+749delinsTG
ENST00000638281.1:c.780+289_780+290delinsTG	ENSP00000491088.1:n.780+289_780+290delinsTG
ENST00000638618.1:c.435+289_435+290delinsTG	ENSP00000492832.1:n.435+289_435+290delinsTG
ENST00000639277.1:c.780+289_780+290delinsTG	ENSP00000492432.1:n.780+289_780+290delinsTG
ENST00000640552.1:n.794+289_794+290delinsTG
ENST00000253408.9:c.780+289_780+290delinsTG	ENSP00000253408.4:n.780+289_780+290delinsTG
ENST00000376990.8:c.*179+289_*179+290delinsTG	ENSP00000366189.4:n.*179+289_*179+290delinsTG
ENST00000435360.6:c.780+289_780+290delinsTG	ENSP00000403962.1:n.780+289_780+290delinsTG
ENST00000586793.5:c.780+289_780+290delinsTG	ENSP00000468500.1:n.780+289_780+290delinsTG
ENST00000587997.5:c.256+289_256+290delinsTG
ENST00000588316.1:c.684+289_684+290delinsTG	ENSP00000465629.1:n.684+289_684+290delinsTG
ENST00000588735.1:c.82+2425_82+2426delinsTG	ENSP00000466598.1:n.82+2425_82+2426delinsTG
ENST00000588957.5:c.48+289_48+290delinsTG	ENSP00000465565.1:n.48+289_48+290delinsTG
ENST00000590922.1:n.430+289_430+290delinsTG
ENST00000592320.5:c.618+748_618+749delinsTG	ENSP00000465320.1:n.618+748_618+749delinsTG
NM_001131019.2:c.780+289_780+290delinsTG	NP_001124491.1:n.780+289_780+290delinsTG
NM_001242376.1:c.780+289_780+290delinsTG	NP_001229305.1:n.780+289_780+290delinsTG
NM_002055.4:c.780+289_780+290delinsTG	NP_002046.1:n.780+289_780+290delinsTG
NM_001363846.1:c.780+289_780+290delinsTG	NP_001350775.1:n.780+289_780+290delinsTG
XM_024450690.1:c.984+289_984+290delinsTG	XP_024306458.1:n.984+289_984+290delinsTG
XM_024450691.1:c.984+289_984+290delinsTG	XP_024306459.1:n.984+289_984+290delinsTG
XM_024450692.1:c.984+289_984+290delinsTG	XP_024306460.1:n.984+289_984+290delinsTG
XM_024450693.1:c.984+289_984+290delinsTG	XP_024306461.1:n.984+289_984+290delinsTG
NM_002055.5:c.780+289_780+290delinsTG MANE Select	NP_002046.1:n.780+289_780+290delinsTG
NM_001131019.3:c.780+289_780+290delinsTG	NP_001124491.1:n.780+289_780+290delinsTG
NM_001242376.2:c.780+289_780+290delinsTG	NP_001229305.1:n.780+289_780+290delinsTG
NM_001242376.3:c.780+289_780+290delinsTG	NP_001229305.1:n.780+289_780+290delinsTG
NM_001363846.2:c.780+289_780+290delinsTG	NP_001350775.1:n.780+289_780+290delinsTG