Canonical Allele Identifier: CA2379515785

Gene: C21orf91

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.17795162T= , CM000683.2:g.17795162T=	GRCh38
NC_000021.8:g.19167479T= , CM000683.1:g.19167479T=	GRCh37
NC_000021.7:g.18089350T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001100420.2:c.727+46A= MANE Select	NP_001093890.1:n.727+46A=
ENST00000284881.9:c.727+46A= MANE Select	ENSP00000284881.4:n.727+46A=
NM_001100420.1:c.727+46A=	NP_001093890.1:n.727+46A=
NM_001100421.1:c.664+1420A=	NP_001093891.1:n.664+1420A=
NM_001100421.2:c.664+1420A=	NP_001093891.1:n.664+1420A=
NM_017447.3:c.727+46A=	NP_059143.3:n.727+46A=
NM_017447.4:c.727+46A=	NP_059143.3:n.727+46A=
ENST00000284881.8:c.727+46A=	ENSP00000284881.4:n.727+46A=
ENST00000400558.7:c.664+1420A=	ENSP00000383403.3:n.664+1420A=
ENST00000400559.7:c.727+46A=	ENSP00000383404.3:n.727+46A=