Canonical Allele Identifier: CA2809605719

Gene: GFAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44908242_44908243insAACACACCCAAC , CM000679.2:g.44908242_44908243insAACACACCCAAC	GRCh38
NC_000017.10:g.42985610_42985611insAACACACCCAAC , CM000679.1:g.42985610_42985611insAACACACCCAAC	GRCh37
NC_000017.9:g.40341136_40341137insAACACACCCAAC	NCBI36
NG_008401.1:g.12304_12305insGTTGGGTGTGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253408.11:c.1292-94_1292-93insGTTGGGTGTGTT	ENSP00000253408.5:n.1292-94_1292-93insGTTGGGTGTGTT
ENST00000253408.10:c.1292-94_1292-93insGTTGGGTGTGTT	ENSP00000253408.5:n.1292-94_1292-93insGTTGGGTGTGTT
ENST00000441312.2:n.25-94_25-93insGTTGGGTGTGTT
ENST00000585543.6:n.325-94_325-93insGTTGGGTGTGTT
ENST00000586125.2:c.107-94_107-93insGTTGGGTGTGTT	ENSP00000467397.2:n.107-94_107-93insGTTGGGTGTGTT
ENST00000588735.3:c.1172-94_1172-93insGTTGGGTGTGTT MANE Select	ENSP00000466598.2:n.1172-94_1172-93insGTTGGGTGTGTT
ENST00000589701.2:n.1985_1986insGTTGGGTGTGTT
ENST00000591880.2:c.271-94_271-93insGTTGGGTGTGTT
ENST00000592065.2:n.446_447insGTTGGGTGTGTT
ENST00000638304.1:c.91-94_91-93insGTTGGGTGTGTT
ENST00000638400.1:c.7-94_7-93insGTTGGGTGTGTT
ENST00000638488.1:n.636-94_636-93insGTTGGGTGTGTT
ENST00000638618.1:c.827-94_827-93insGTTGGGTGTGTT	ENSP00000492832.1:n.827-94_827-93insGTTGGGTGTGTT
ENST00000638921.1:n.5_6insGTTGGGTGTGTT
ENST00000639042.1:c.144-94_144-93insGTTGGGTGTGTT
ENST00000639277.1:c.1172-94_1172-93insGTTGGGTGTGTT	ENSP00000492432.1:n.1172-94_1172-93insGTTGGGTGTGTT
ENST00000639369.1:c.22-94_22-93insGTTGGGTGTGTT
ENST00000640552.1:n.3557_3558insGTTGGGTGTGTT
ENST00000253408.9:c.1172-94_1172-93insGTTGGGTGTGTT	ENSP00000253408.4:n.1172-94_1172-93insGTTGGGTGTGTT
ENST00000585543.5:n.325-94_325-93insGTTGGGTGTGTT
ENST00000586125.1:c.143-94_143-93insGTTGGGTGTGTT	ENSP00000467397.1:n.143-94_143-93insGTTGGGTGTGTT
ENST00000588640.5:n.552-94_552-93insGTTGGGTGTGTT
ENST00000588735.1:c.83-127_83-126insGTTGGGTGTGTT	ENSP00000466598.1:n.83-127_83-126insGTTGGGTGTGTT
ENST00000591880.1:c.38-94_38-93insGTTGGGTGTGTT	ENSP00000467530.1:n.38-94_38-93insGTTGGGTGTGTT
ENST00000592706.5:n.44-94_44-93insGTTGGGTGTGTT
NM_002055.4:c.1172-94_1172-93insGTTGGGTGTGTT	NP_002046.1:n.1172-94_1172-93insGTTGGGTGTGTT
NM_001363846.1:c.1292-94_1292-93insGTTGGGTGTGTT	NP_001350775.1:n.1292-94_1292-93insGTTGGGTGTGTT
XM_024450690.1:c.1496-94_1496-93insGTTGGGTGTGTT	XP_024306458.1:n.1496-94_1496-93insGTTGGGTGTGTT
XM_024450692.1:c.1376-94_1376-93insGTTGGGTGTGTT	XP_024306460.1:n.1376-94_1376-93insGTTGGGTGTGTT
NM_002055.5:c.1172-94_1172-93insGTTGGGTGTGTT MANE Select	NP_002046.1:n.1172-94_1172-93insGTTGGGTGTGTT
NM_001242376.2:c.*2226_*2227insGTTGGGTGTGTT	NP_001229305.1:n.*2226_*2227insGTTGGGTGTGTT
NM_001363846.2:c.1292-94_1292-93insGTTGGGTGTGTT	NP_001350775.1:n.1292-94_1292-93insGTTGGGTGTGTT