Canonical Allele Identifier: CA9983472

Gene: C21orf91

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.17796901G>C , CM000683.2:g.17796901G>C	GRCh38
NC_000021.8:g.19169218G>C , CM000683.1:g.19169218G>C	GRCh37
NC_000021.7:g.18091089G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284881.9:c.345C>G MANE Select	ENSP00000284881.4:p.Asn115Lys
ENST00000284881.8:c.345C>G	ENSP00000284881.4:p.Asn115Lys
ENST00000400558.7:c.345C>G	ENSP00000383403.3:p.Asn115Lys
ENST00000400559.7:c.345C>G	ENSP00000383404.3:p.Asn115Lys
ENST00000405964.2:c.345C>G	ENSP00000385566.2:p.Asn115Lys
ENST00000493464.1:n.566C>G
NM_001100420.1:c.345C>G	NP_001093890.1:p.Asn115Lys
NM_001100421.1:c.345C>G	NP_001093891.1:p.Asn115Lys
NM_017447.3:c.345C>G	NP_059143.3:p.Asn115Lys
NM_001100420.2:c.345C>G MANE Select	NP_001093890.1:p.Asn115Lys
NM_001100421.2:c.345C>G	NP_001093891.1:p.Asn115Lys
NM_017447.4:c.345C>G	NP_059143.3:p.Asn115Lys