Canonical Allele Identifier: CA15590701
Gene: C9orf72 HGNC NCBI

Linked Data

dbSNP Id: rs774359
gnomAD v2: 9-27561049-T-C
gnomAD v3: 9-27561051-T-C
gnomAD v4: 9-27561051-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.27561051T>C , CM000671.2:g.27561051T>C GRCh38
NC_000009.11:g.27561049T>C , CM000671.1:g.27561049T>C GRCh37
NC_000009.10:g.27551049T>C NCBI36
NG_031977.1:g.17816A>G
NG_031977.2:g.17816A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000380003.8:c.665+534A>G MANE Select ENSP00000369339.3:n.665+534A>G
ENST00000619707.5:c.665+534A>G ENSP00000482753.1:n.665+534A>G
ENST00000644136.1:c.665+534A>G ENSP00000494872.1:n.665+534A>G
ENST00000647196.1:c.665+534A>G ENSP00000494839.1:n.665+534A>G
ENST00000673600.1:c.665+534A>G ENSP00000500650.1:n.665+534A>G
ENST00000379997.7:c.*530A>G ENSP00000369333.3:n.*530A>G
ENST00000380003.7:c.665+534A>G ENSP00000369339.3:n.665+534A>G
ENST00000488117.5:n.727+534A>G
ENST00000619707.4:c.665+534A>G ENSP00000482753.1:n.665+534A>G
NM_001256054.2:c.665+534A>G NP_001242983.1:n.665+534A>G
NM_018325.4:c.665+534A>G NP_060795.1:n.665+534A>G
NM_145005.6:c.*530A>G NP_659442.2:n.*530A>G
NM_018325.5:c.665+534A>G MANE Select NP_060795.1:n.665+534A>G
NM_001256054.3:c.665+534A>G NP_001242983.1:n.665+534A>G
NM_145005.7:c.*530A>G NP_659442.2:n.*530A>G