Canonical Allele Identifier: CA219267

Gene: SERPING1

Linked Data

• ClinVar Variation Id: 68253
• ClinVar RCV Id: RCV000059091 ; RCV000768681
• dbSNP Id: rs281875170
• COSMIC: COSM4034076
• MyVariant Identifiers: chr11:g.57367850G>A (hg19) ; chr11:g.57600377G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57600377G>A , CM000673.2:g.57600377G>A	GRCh38
NC_000011.9:g.57367850G>A , CM000673.1:g.57367850G>A	GRCh37
NC_000011.8:g.57124426G>A	NCBI36
NG_009625.1:g.7824G>A , LRG_105:g.7824G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.550G>A MANE Select	ENSP00000278407.4:p.Gly184Arg
ENST00000528996.2:c.58+2049G>A	ENSP00000431226.2:n.58+2049G>A
ENST00000531605.2:c.52-1658G>A	ENSP00000503752.1:n.52-1658G>A
ENST00000619430.2:c.550G>A	ENSP00000478572.2:p.Gly184Arg
ENST00000676670.1:c.550G>A	ENSP00000504807.1:p.Gly184Arg
ENST00000676741.1:n.1632G>A
ENST00000677275.1:n.537G>A
ENST00000677624.1:c.550G>A	ENSP00000503979.1:p.Gly184Arg
ENST00000677625.1:c.550G>A	ENSP00000502857.1:p.Gly184Arg
ENST00000677856.1:n.609G>A
ENST00000677915.1:c.550G>A	ENSP00000503118.1:p.Gly184Arg
ENST00000678533.1:c.52-1658G>A	ENSP00000503873.1:n.52-1658G>A
ENST00000678592.1:c.550G>A	ENSP00000504424.1:p.Gly184Arg
ENST00000278407.8:c.550G>A	ENSP00000278407.4:p.Gly184Arg
ENST00000340687.10:c.550G>A	ENSP00000341861.6:p.Gly184Arg
ENST00000378323.8:c.565G>A	ENSP00000367574.4:p.Gly189Arg
ENST00000378324.6:c.394G>A	ENSP00000367575.2:p.Gly132Arg
ENST00000403558.1:c.652G>A	ENSP00000384420.1:p.Gly218Arg
ENST00000531133.5:c.52-1658G>A	ENSP00000435431.1:n.52-1658G>A
ENST00000531797.5:c.52-1658G>A	ENSP00000432554.1:n.52-1658G>A
ENST00000619430.1:c.348+202G>A	ENSP00000478572.1:n.348+202G>A
NM_000062.2:c.550G>A , LRG_105t1:c.550G>A	NP_000053.2:p.Gly184Arg
NM_001032295.1:c.550G>A	NP_001027466.1:p.Gly184Arg
NM_000062.3:c.550G>A MANE Select	NP_000053.2:p.Gly184Arg
NM_001032295.2:c.550G>A	NP_001027466.1:p.Gly184Arg