Canonical Allele Identifier: CA1992462659
Gene: C11orf97 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94522161G= , CM000673.2:g.94522161G= GRCh38
NC_000011.9:g.94255327G= , CM000673.1:g.94255327G= GRCh37
NC_000011.8:g.93894975G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000542198.3:c.250+4474G= MANE Select ENSP00000490577.1:n.250+4474G=
NM_001190462.1:c.250+4474G= NP_001177391.1:n.250+4474G=
NM_001190462.2:c.250+4474G= MANE Select NP_001177391.1:n.250+4474G=
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