Canonical Allele Identifier: CA682090716

Gene: C11orf97

Linked Data

• dbSNP Id: rs1264305199
• MyVariant Identifiers: chr11:g.94255315_94255327del (hg19) ; chr11:g.94522149_94522161del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94522151_94522163del , CM000673.2:g.94522151_94522163del	GRCh38
NC_000011.9:g.94255317_94255329del , CM000673.1:g.94255317_94255329del	GRCh37
NC_000011.8:g.93894965_93894977del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542198.3:c.250+4464_250+4476del MANE Select	ENSP00000490577.1:n.250+4464_250+4476del
NM_001190462.1:c.250+4464_250+4476del	NP_001177391.1:n.250+4464_250+4476del
NM_001190462.2:c.250+4464_250+4476del MANE Select	NP_001177391.1:n.250+4464_250+4476del