Canonical Allele Identifier: CA2261610111

Gene: GFAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44907817_44907821delinsAAGAG , CM000679.2:g.44907817_44907821delinsAAGAG	GRCh38
NC_000017.10:g.42985185_42985189delinsAAGAG , CM000679.1:g.42985185_42985189delinsAAGAG	GRCh37
NC_000017.9:g.40340711_40340715delinsAAGAG	NCBI36
NG_008401.1:g.12726_12730delinsCTCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253408.11:c.1377+243_1377+247delinsCTCTT	ENSP00000253408.5:n.1377+243_1377+247delinsCTCTT
ENST00000253408.10:c.1377+243_1377+247delinsCTCTT	ENSP00000253408.5:n.1377+243_1377+247delinsCTCTT
ENST00000441312.2:n.110+243_110+247delinsCTCTT
ENST00000585543.6:n.410+243_410+247delinsCTCTT
ENST00000586125.2:c.435_439delinsCTCTT	ENSP00000467397.2:n.435_439delinsCTCTT
ENST00000588735.3:c.1257+243_1257+247delinsCTCTT MANE Select	ENSP00000466598.2:n.1257+243_1257+247delinsCTCTT
ENST00000589701.2:n.2164+243_2164+247delinsCTCTT
ENST00000591880.2:c.599_603delinsCTCTT
ENST00000592065.2:n.625+243_625+247delinsCTCTT
ENST00000638304.1:c.176+243_176+247delinsCTCTT
ENST00000638400.1:c.92+243_92+247delinsCTCTT
ENST00000638488.1:n.721+243_721+247delinsCTCTT
ENST00000638618.1:c.912+243_912+247delinsCTCTT	ENSP00000492832.1:n.912+243_912+247delinsCTCTT
ENST00000638921.1:n.427_431delinsCTCTT
ENST00000639042.1:c.229+243_229+247delinsCTCTT
ENST00000639243.1:c.13+243_13+247delinsCTCTT
ENST00000639277.1:c.1257+243_1257+247delinsCTCTT	ENSP00000492432.1:n.1257+243_1257+247delinsCTCTT
ENST00000639369.1:c.107+243_107+247delinsCTCTT
ENST00000640545.1:c.63+243_63+247delinsCTCTT	ENSP00000491735.1:n.63+243_63+247delinsCTCTT
ENST00000640859.1:c.71+243_71+247delinsCTCTT
ENST00000253408.9:c.1257+243_1257+247delinsCTCTT	ENSP00000253408.4:n.1257+243_1257+247delinsCTCTT
ENST00000585543.5:n.410+243_410+247delinsCTCTT
ENST00000588735.1:c.135+243_135+247delinsCTCTT	ENSP00000466598.1:n.135+243_135+247delinsCTCTT
ENST00000589701.1:n.159+243_159+247delinsCTCTT
ENST00000591880.1:c.366_370delinsCTCTT	ENSP00000467530.1:n.366_370delinsCTCTT
ENST00000592065.1:n.51+243_51+247delinsCTCTT
ENST00000592706.5:n.129+243_129+247delinsCTCTT
NM_002055.4:c.1257+243_1257+247delinsCTCTT	NP_002046.1:n.1257+243_1257+247delinsCTCTT
NM_001363846.1:c.1377+243_1377+247delinsCTCTT	NP_001350775.1:n.1377+243_1377+247delinsCTCTT
XM_024450690.1:c.1581+243_1581+247delinsCTCTT	XP_024306458.1:n.1581+243_1581+247delinsCTCTT
XM_024450692.1:c.1461+243_1461+247delinsCTCTT	XP_024306460.1:n.1461+243_1461+247delinsCTCTT
NM_002055.5:c.1257+243_1257+247delinsCTCTT MANE Select	NP_002046.1:n.1257+243_1257+247delinsCTCTT
NM_001363846.2:c.1377+243_1377+247delinsCTCTT	NP_001350775.1:n.1377+243_1377+247delinsCTCTT