Canonical Allele Identifier: CA2379514504

Gene: C21orf91 C21orf91-OT1

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.17792325A= , CM000683.2:g.17792325A=	GRCh38
NC_000021.8:g.19164642A= , CM000683.1:g.19164642A=	GRCh37
NC_000021.7:g.18086513A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001100420.2:c.*1090T= (C21orf91) MANE Select	NP_001093890.1:n.*1090T=
ENST00000284881.9:c.*1090T= (C21orf91) MANE Select	ENSP00000284881.4:n.*1090T=
NM_001100420.1:c.*1090T= (C21orf91)	NP_001093890.1:n.*1090T=
NM_001100421.1:c.*1255T= (C21orf91)	NP_001093891.1:n.*1255T=
NM_001100421.2:c.*1255T= (C21orf91)	NP_001093891.1:n.*1255T=
NM_017447.3:c.*1090T= (C21orf91)	NP_059143.3:n.*1090T=
NM_017447.4:c.*1090T= (C21orf91)	NP_059143.3:n.*1090T=
NR_038870.1:n.33+152T= (C21orf91-OT1)
NR_038871.1:n.33+152T= (C21orf91-OT1)
ENST00000284881.8:c.*1090T= (C21orf91)	ENSP00000284881.4:n.*1090T=