Canonical Allele Identifier: CA380690795

Gene: SERPING1

Linked Data

• dbSNP Id: rs1945516584
• MyVariant Identifiers: chr11:g.57381975A>G (hg19) ; chr11:g.57614502A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614502A>G , CM000673.2:g.57614502A>G	GRCh38
NC_000011.9:g.57381975A>G , CM000673.1:g.57381975A>G	GRCh37
NC_000011.8:g.57138551A>G	NCBI36
NG_009625.1:g.21949A>G , LRG_105:g.21949A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1424A>G MANE Select	ENSP00000278407.4:p.Gln475Arg
ENST00000528996.2:c.*321A>G	ENSP00000431226.2:n.*321A>G
ENST00000531605.2:c.*1200A>G	ENSP00000503752.1:n.*1200A>G
ENST00000619430.2:c.1220A>G	ENSP00000478572.2:p.Gln407Arg
ENST00000676670.1:c.1424A>G	ENSP00000504807.1:p.Gln475Arg
ENST00000676741.1:n.2506A>G
ENST00000677624.1:c.*844A>G	ENSP00000503979.1:n.*844A>G
ENST00000677625.1:c.1370A>G	ENSP00000502857.1:p.Gln457Arg
ENST00000677856.1:n.1677A>G
ENST00000677915.1:c.*321A>G	ENSP00000503118.1:n.*321A>G
ENST00000678533.1:c.*978A>G	ENSP00000503873.1:n.*978A>G
ENST00000678592.1:c.*364A>G	ENSP00000504424.1:n.*364A>G
ENST00000278407.8:c.1424A>G	ENSP00000278407.4:p.Gln475Arg
ENST00000340687.10:c.1313A>G	ENSP00000341861.6:p.Gln438Arg
ENST00000378323.8:c.1439A>G	ENSP00000367574.4:p.Gln480Arg
ENST00000378324.6:c.1268A>G	ENSP00000367575.2:p.Gln423Arg
ENST00000403558.1:c.1553A>G	ENSP00000384420.1:p.Gln518Arg
ENST00000528996.1:c.625A>G	ENSP00000431226.1:n.625A>G
ENST00000530113.1:n.881A>G
ENST00000531133.5:c.925A>G	ENSP00000435431.1:n.925A>G
ENST00000531797.5:c.*449A>G	ENSP00000432554.1:n.*449A>G
ENST00000619430.1:c.555A>G	ENSP00000478572.1:n.555A>G
NM_000062.2:c.1424A>G , LRG_105t1:c.1424A>G	NP_000053.2:p.Gln475Arg
NM_001032295.1:c.1424A>G	NP_001027466.1:p.Gln475Arg
NM_000062.3:c.1424A>G MANE Select	NP_000053.2:p.Gln475Arg
NM_001032295.2:c.1424A>G	NP_001027466.1:p.Gln475Arg