Canonical Allele Identifier: CA320609

Gene: COX20

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244835721G>T , CM000663.2:g.244835721G>T	GRCh38
NC_000001.10:g.244999023G>T , CM000663.1:g.244999023G>T	GRCh37
NC_000001.9:g.243065646G>T	NCBI36
NG_042825.1:g.5416G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411948.7:c.7G>T MANE Select	ENSP00000406327.2:p.Ala3Ser
ENST00000366528.3:c.7G>T	ENSP00000355486.3:p.Ala3Ser
ENST00000391839.6:n.66G>T
ENST00000411948.6:c.7G>T	ENSP00000406327.2:p.Ala3Ser
ENST00000498262.1:n.63G>T
NM_001312871.1:c.7G>T	NP_001299800.1:p.Ala3Ser
NM_001312872.1:c.7G>T	NP_001299801.1:p.Ala3Ser
NM_001312873.1:c.7G>T	NP_001299802.1:p.Ala3Ser
NM_001312874.1:c.7G>T	NP_001299803.1:p.Ala3Ser
NM_198076.4:c.7G>T	NP_932342.1:p.Ala3Ser
NM_198076.5:c.7G>T	NP_932342.1:p.Ala3Ser
NR_132419.1:n.246G>T
NR_132420.1:n.246G>T
NR_132421.1:n.246G>T
NM_198076.6:c.7G>T MANE Select	NP_932342.1:p.Ala3Ser