Canonical Allele Identifier: CA1992462592

Gene: C11orf97

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94522114_94522115delinsAT , CM000673.2:g.94522114_94522115delinsAT	GRCh38
NC_000011.9:g.94255280_94255281delinsAT , CM000673.1:g.94255280_94255281delinsAT	GRCh37
NC_000011.8:g.93894928_93894929delinsAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542198.3:c.250+4427_250+4428delinsAT MANE Select	ENSP00000490577.1:n.250+4427_250+4428delinsAT
NM_001190462.1:c.250+4427_250+4428delinsAT	NP_001177391.1:n.250+4427_250+4428delinsAT
NM_001190462.2:c.250+4427_250+4428delinsAT MANE Select	NP_001177391.1:n.250+4427_250+4428delinsAT