Canonical Allele Identifier: CA2274501195

Gene: SDK2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.73339121G= , CM000679.2:g.73339121G=	GRCh38
NC_000017.10:g.71335260G= , CM000679.1:g.71335260G=	GRCh37
NC_000017.9:g.68846855G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001144952.2:c.6166-181C= MANE Select	NP_001138424.1:n.6166-181C=
ENST00000392650.8:c.6166-181C= MANE Select	ENSP00000376421.3:n.6166-181C=
NM_001144952.1:c.6166-181C=	NP_001138424.1:n.6166-181C=
ENST00000392650.7:c.6166-181C=	ENSP00000376421.3:n.6166-181C=
ENST00000410094.5:n.1239-181C=
ENST00000424778.1:c.3637-181C=	ENSP00000407098.1:n.3637-181C=
XM_011524914.1:c.6109-181C=	XP_011523216.1:n.6109-181C=
XM_011524914.2:c.6109-181C=	XP_011523216.1:n.6109-181C=
XM_011524915.1:c.6166-181C=	XP_011523217.1:n.6166-181C=
XM_011524915.2:c.6166-181C=	XP_011523217.1:n.6166-181C=