Canonical Allele Identifier: CA2261610326
Gene: GFAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44908275_44908303delinsAGAGAGCCTAGGCTCTTCCAAACGGGCTG , CM000679.2:g.44908275_44908303delinsAGAGAGCCTAGGCTCTTCCAAACGGGCTG GRCh38
NC_000017.10:g.42985643_42985671delinsAGAGAGCCTAGGCTCTTCCAAACGGGCTG , CM000679.1:g.42985643_42985671delinsAGAGAGCCTAGGCTCTTCCAAACGGGCTG GRCh37
NC_000017.9:g.40341169_40341197delinsAGAGAGCCTAGGCTCTTCCAAACGGGCTG NCBI36
NG_008401.1:g.12244_12272delinsCAGCCCGTTTGGAAGAGCCTAGGCTCTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000253408.11:c.1292-154_1292-126delinsCAGCCCGTTTGGAAGAGCCTAGGCTCTCT ENSP00000253408.5:n.1292-154_1292-126delinsCAGCCCGTTTGGAAGAGC...
ENST00000253408.10:c.1292-154_1292-126delinsCAGCCCGTTTGGAAGAGCCTAGGCTCTCT ENSP00000253408.5:n.1292-154_1292-126delinsCAGCCCGTTTGGAAGAGC...
ENST00000441312.2:n.25-154_25-126delinsCAGCCCGTTTGGAAGAGCCTAGGCTCTCT
ENST00000585543.6:n.325-154_325-126delinsCAGCCCGTTTGGAAGAGCCTAGGCTCTCT
ENST00000586125.2:c.107-154_107-126delinsCAGCCCGTTTGGAAGAGCCTAGGCTCTCT ENSP00000467397.2:n.107-154_107-126delinsCAGCCCGTTTGGAAGAGCCT...
ENST00000588735.3:c.1172-154_1172-126delinsCAGCCCGTTTGGAAGAGCCTAGGCTCTCT MANE Select ENSP00000466598.2:n.1172-154_1172-126delinsCAGCCCGTTTGGAAGAGC...
ENST00000589701.2:n.1925_1953delinsCAGCCCGTTTGGAAGAGCCTAGGCTCTCT
ENST00000591880.2:c.271-154_271-126delinsCAGCCCGTTTGGAAGAGCCTAGGCTCTCT
ENST00000592065.2:n.386_414delinsCAGCCCGTTTGGAAGAGCCTAGGCTCTCT
ENST00000638304.1:c.91-154_91-126delinsCAGCCCGTTTGGAAGAGCCTAGGCTCTCT
ENST00000638400.1:c.7-154_7-126delinsCAGCCCGTTTGGAAGAGCCTAGGCTCTCT
ENST00000638488.1:n.636-154_636-126delinsCAGCCCGTTTGGAAGAGCCTAGGCTCTCT
ENST00000638618.1:c.827-154_827-126delinsCAGCCCGTTTGGAAGAGCCTAGGCTCTCT ENSP00000492832.1:n.827-154_827-126delinsCAGCCCGTTTGGAAGAGCCT...
ENST00000639042.1:c.144-154_144-126delinsCAGCCCGTTTGGAAGAGCCTAGGCTCTCT
ENST00000639277.1:c.1172-154_1172-126delinsCAGCCCGTTTGGAAGAGCCTAGGCTCTCT ENSP00000492432.1:n.1172-154_1172-126delinsCAGCCCGTTTGGAAGAGC...
ENST00000639369.1:c.22-154_22-126delinsCAGCCCGTTTGGAAGAGCCTAGGCTCTCT
ENST00000640552.1:n.3497_3525delinsCAGCCCGTTTGGAAGAGCCTAGGCTCTCT
ENST00000253408.9:c.1172-154_1172-126delinsCAGCCCGTTTGGAAGAGCCTAGGCTCTCT ENSP00000253408.4:n.1172-154_1172-126delinsCAGCCCGTTTGGAAGAGC...
ENST00000585543.5:n.325-154_325-126delinsCAGCCCGTTTGGAAGAGCCTAGGCTCTCT
ENST00000586125.1:c.143-154_143-126delinsCAGCCCGTTTGGAAGAGCCTAGGCTCTCT ENSP00000467397.1:n.143-154_143-126delinsCAGCCCGTTTGGAAGAGCCT...
ENST00000588640.5:n.552-154_552-126delinsCAGCCCGTTTGGAAGAGCCTAGGCTCTCT
ENST00000588735.1:c.83-187_83-159delinsCAGCCCGTTTGGAAGAGCCTAGGCTCTCT ENSP00000466598.1:n.83-187_83-159delinsCAGCCCGTTTGGAAGAGCCTAG...
ENST00000591880.1:c.38-154_38-126delinsCAGCCCGTTTGGAAGAGCCTAGGCTCTCT ENSP00000467530.1:n.38-154_38-126delinsCAGCCCGTTTGGAAGAGCCTAG...
ENST00000592706.5:n.44-154_44-126delinsCAGCCCGTTTGGAAGAGCCTAGGCTCTCT
NM_002055.4:c.1172-154_1172-126delinsCAGCCCGTTTGGAAGAGCCTAGGCTCTCT NP_002046.1:n.1172-154_1172-126delinsCAGCCCGTTTGGAAGAGCCTAGGC...
NM_001363846.1:c.1292-154_1292-126delinsCAGCCCGTTTGGAAGAGCCTAGGCTCTCT NP_001350775.1:n.1292-154_1292-126delinsCAGCCCGTTTGGAAGAGCCTA...
XM_024450690.1:c.1496-154_1496-126delinsCAGCCCGTTTGGAAGAGCCTAGGCTCTCT XP_024306458.1:n.1496-154_1496-126delinsCAGCCCGTTTGGAAGAGCCTA...
XM_024450692.1:c.1376-154_1376-126delinsCAGCCCGTTTGGAAGAGCCTAGGCTCTCT XP_024306460.1:n.1376-154_1376-126delinsCAGCCCGTTTGGAAGAGCCTA...
NM_002055.5:c.1172-154_1172-126delinsCAGCCCGTTTGGAAGAGCCTAGGCTCTCT MANE Select NP_002046.1:n.1172-154_1172-126delinsCAGCCCGTTTGGAAGAGCCTAGGC...
NM_001242376.2:c.*2166_*2194delinsCAGCCCGTTTGGAAGAGCCTAGGCTCTCT NP_001229305.1:n.*2166_*2194delinsCAGCCCGTTTGGAAGAGCCTAGGCTCT...
NM_001363846.2:c.1292-154_1292-126delinsCAGCCCGTTTGGAAGAGCCTAGGCTCTCT NP_001350775.1:n.1292-154_1292-126delinsCAGCCCGTTTGGAAGAGCCTA...