Canonical Allele Identifier: CA16603677

Gene: COX20

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244835755A>G , CM000663.2:g.244835755A>G	GRCh38
NC_000001.10:g.244999057A>G , CM000663.1:g.244999057A>G	GRCh37
NC_000001.9:g.243065680A>G	NCBI36
NG_042825.1:g.5450A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411948.7:c.41A>G MANE Select	ENSP00000406327.2:p.Lys14Arg
ENST00000366528.3:c.41A>G	ENSP00000355486.3:p.Lys14Arg
ENST00000391839.6:n.100A>G
ENST00000411948.6:c.41A>G	ENSP00000406327.2:p.Lys14Arg
ENST00000498262.1:n.97A>G
NM_001312871.1:c.41A>G	NP_001299800.1:p.Lys14Arg
NM_001312872.1:c.41A>G	NP_001299801.1:p.Lys14Arg
NM_001312873.1:c.22+19A>G	NP_001299802.1:n.22+19A>G
NM_001312874.1:c.41A>G	NP_001299803.1:p.Lys14Arg
NM_198076.4:c.41A>G	NP_932342.1:p.Lys14Arg
NM_198076.5:c.41A>G	NP_932342.1:p.Lys14Arg
NR_132419.1:n.280A>G
NR_132420.1:n.261+19A>G
NR_132421.1:n.261+19A>G
NM_198076.6:c.41A>G MANE Select	NP_932342.1:p.Lys14Arg