Canonical Allele Identifier: CA2838565128

Gene: GFAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44911512_44911513del , CM000679.2:g.44911512_44911513del	GRCh38
NC_000017.10:g.42988880_42988881del , CM000679.1:g.42988880_42988881del	GRCh37
NC_000017.9:g.40344406_40344407del	NCBI36
NG_008401.1:g.9034_9035del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253408.11:c.907-57_907-56del	ENSP00000253408.5:n.907-57_907-56del
ENST00000435360.8:c.907-57_907-56del	ENSP00000403962.1:n.907-57_907-56del
ENST00000253408.10:c.907-57_907-56del	ENSP00000253408.5:n.907-57_907-56del
ENST00000435360.7:c.907-57_907-56del	ENSP00000403962.1:n.907-57_907-56del
ENST00000585543.6:n.3_4del
ENST00000586127.6:n.1436-57_1436-56del
ENST00000586793.6:c.906+159_906+160del	ENSP00000468500.2:n.906+159_906+160del
ENST00000587997.6:n.383-57_383-56del
ENST00000588735.3:c.907-57_907-56del MANE Select	ENSP00000466598.2:n.907-57_907-56del
ENST00000591327.2:n.2061-57_2061-56del
ENST00000592320.6:c.619-192_619-191del	ENSP00000465320.1:n.619-192_619-191del
ENST00000638281.1:c.907-57_907-56del	ENSP00000491088.1:n.907-57_907-56del
ENST00000638618.1:c.562-57_562-56del	ENSP00000492832.1:n.562-57_562-56del
ENST00000639277.1:c.907-57_907-56del	ENSP00000492432.1:n.907-57_907-56del
ENST00000640552.1:n.921-57_921-56del
ENST00000253408.9:c.907-57_907-56del	ENSP00000253408.4:n.907-57_907-56del
ENST00000376990.8:c.*306-57_*306-56del	ENSP00000366189.4:n.*306-57_*306-56del
ENST00000435360.6:c.907-57_907-56del	ENSP00000403962.1:n.907-57_907-56del
ENST00000585543.5:n.3_4del
ENST00000586793.5:c.907-57_907-56del	ENSP00000468500.1:n.907-57_907-56del
ENST00000587997.5:c.383-57_383-56del
ENST00000588640.5:n.287-57_287-56del
ENST00000588735.1:c.83-3397_83-3396del	ENSP00000466598.1:n.83-3397_83-3396del
ENST00000591719.5:n.541-57_541-56del
ENST00000592320.5:c.619-192_619-191del	ENSP00000465320.1:n.619-192_619-191del
NM_001131019.2:c.907-57_907-56del	NP_001124491.1:n.907-57_907-56del
NM_001242376.1:c.907-57_907-56del	NP_001229305.1:n.907-57_907-56del
NM_002055.4:c.907-57_907-56del	NP_002046.1:n.907-57_907-56del
NM_001363846.1:c.907-57_907-56del	NP_001350775.1:n.907-57_907-56del
XM_024450690.1:c.1111-57_1111-56del	XP_024306458.1:n.1111-57_1111-56del
XM_024450691.1:c.1111-57_1111-56del	XP_024306459.1:n.1111-57_1111-56del
XM_024450692.1:c.1111-57_1111-56del	XP_024306460.1:n.1111-57_1111-56del
XM_024450693.1:c.1111-57_1111-56del	XP_024306461.1:n.1111-57_1111-56del
NM_002055.5:c.907-57_907-56del MANE Select	NP_002046.1:n.907-57_907-56del
NM_001131019.3:c.907-57_907-56del	NP_001124491.1:n.907-57_907-56del
NM_001242376.2:c.907-57_907-56del	NP_001229305.1:n.907-57_907-56del
NM_001242376.3:c.907-57_907-56del	NP_001229305.1:n.907-57_907-56del
NM_001363846.2:c.907-57_907-56del	NP_001350775.1:n.907-57_907-56del