Canonical Allele Identifier: CA2224956043

Gene: CSNK2A2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.58175276A= , CM000678.2:g.58175276A=	GRCh38
NC_000016.9:g.58209180A= , CM000678.1:g.58209180A=	GRCh37
NC_000016.8:g.56766681A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262506.8:c.370-766T= MANE Select	ENSP00000262506.3:n.370-766T=
ENST00000563307.2:n.2179-766T=
ENST00000565188.2:c.217-766T=	ENSP00000454874.2:n.217-766T=
ENST00000677823.1:n.2179-766T=
ENST00000262506.7:c.370-766T=	ENSP00000262506.3:n.370-766T=
ENST00000562367.1:n.195-766T=
ENST00000565188.1:c.370-766T=	ENSP00000454874.1:n.370-766T=
ENST00000566813.5:n.422-766T=
ENST00000567730.6:c.154-7481T=	ENSP00000456606.2:n.154-7481T=
NM_001896.2:c.370-766T=	NP_001887.1:n.370-766T=
XM_005255800.2:c.217-766T=	XP_005255857.1:n.217-766T=
XM_005255801.2:c.-42-766T=	XP_005255858.1:n.-42-766T=
NM_001896.3:c.370-766T=	NP_001887.1:n.370-766T=
XM_005255800.4:c.217-766T=	XP_005255857.1:n.217-766T=
XM_005255801.3:c.-42-766T=	XP_005255858.1:n.-42-766T=
NM_001896.4:c.370-766T= MANE Select	NP_001887.1:n.370-766T=