Canonical Allele Identifier: CA2202125411

Gene: DNASE1L2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2237554C= , CM000678.2:g.2237554C=	GRCh38
NC_000016.9:g.2287555C= , CM000678.1:g.2287555C=	GRCh37
NC_000016.8:g.2227556C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000320700.10:c.496C= MANE Select	ENSP00000316938.5:p.Leu166=
ENST00000320700.9:c.496C=	ENSP00000316938.5:p.Leu166=
ENST00000382437.8:c.433C=	ENSP00000371874.4:p.Leu145=
ENST00000564065.5:c.496C=	ENSP00000454562.1:p.Leu166=
ENST00000567494.5:c.496C=	ENSP00000455358.1:p.Leu166=
ENST00000569184.1:c.487C=	ENSP00000455478.1:p.Leu163=
ENST00000613572.4:c.433C=	ENSP00000482627.1:p.Leu145=
NM_001301680.1:c.496C=	NP_001288609.1:p.Leu166=
NM_001374.2:c.496C=	NP_001365.1:p.Leu166=
XM_011522399.1:c.769C=	XP_011520701.1:p.Leu257=
XM_011522399.2:c.769C=	XP_011520701.1:p.Leu257=
NM_001374.3:c.496C= MANE Select	NP_001365.1:p.Leu166=
NM_001301680.2:c.496C=	NP_001288609.1:p.Leu166=