Canonical Allele Identifier: CA394335216

Gene: DNASE1L2

Linked Data

• MyVariant Identifiers: chr16:g.2287550T>G (hg19) ; chr16:g.2237549T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2237549T>G , CM000678.2:g.2237549T>G	GRCh38
NC_000016.9:g.2287550T>G , CM000678.1:g.2287550T>G	GRCh37
NC_000016.8:g.2227551T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320700.10:c.491T>G MANE Select	ENSP00000316938.5:p.Leu164Arg
ENST00000320700.9:c.491T>G	ENSP00000316938.5:p.Leu164Arg
ENST00000382437.8:c.428T>G	ENSP00000371874.4:p.Leu143Arg
ENST00000564065.5:c.491T>G	ENSP00000454562.1:p.Leu164Arg
ENST00000567494.5:c.491T>G	ENSP00000455358.1:p.Leu164Arg
ENST00000569184.1:c.482T>G	ENSP00000455478.1:p.Leu161Arg
ENST00000613572.4:c.428T>G	ENSP00000482627.1:p.Leu143Arg
NM_001301680.1:c.491T>G	NP_001288609.1:p.Leu164Arg
NM_001374.2:c.491T>G	NP_001365.1:p.Leu164Arg
XM_011522399.1:c.764T>G	XP_011520701.1:p.Leu255Arg
XM_011522399.2:c.764T>G	XP_011520701.1:p.Leu255Arg
NM_001374.3:c.491T>G MANE Select	NP_001365.1:p.Leu164Arg
NM_001301680.2:c.491T>G	NP_001288609.1:p.Leu164Arg