Canonical Allele Identifier: CA10638774

Gene: SERPING1

Linked Data

• ClinVar Variation Id: 305012
• ClinVar RCV Id: RCV000352407
• dbSNP Id: rs886048398
• MyVariant Identifiers: chr11:g.57365162T>G (hg19) ; chr11:g.57597689T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57597689T>G , CM000673.2:g.57597689T>G	GRCh38
NC_000011.9:g.57365162T>G , CM000673.1:g.57365162T>G	GRCh37
NC_000011.8:g.57121738T>G	NCBI36
NG_009625.1:g.5136T>G , LRG_105:g.5136T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.-56T>G MANE Select	ENSP00000278407.4:n.-56T>G
ENST00000619430.2:c.-56T>G	ENSP00000478572.2:n.-56T>G
ENST00000677275.1:n.5T>G
ENST00000677624.1:c.-56T>G	ENSP00000503979.1:n.-56T>G
ENST00000677856.1:n.4T>G
ENST00000677915.1:c.-56T>G	ENSP00000503118.1:n.-56T>G
ENST00000278407.8:c.-56T>G	ENSP00000278407.4:n.-56T>G
ENST00000340687.10:c.-56T>G	ENSP00000341861.6:n.-56T>G
ENST00000378323.8:c.-56T>G	ENSP00000367574.4:n.-56T>G
ENST00000405496.5:c.-23+158T>G	ENSP00000384561.1:n.-23+158T>G
ENST00000457869.1:c.-194T>G	ENSP00000399746.1:n.-194T>G
NM_000062.2:c.-56T>G , LRG_105t1:c.-56T>G	NP_000053.2:n.-56T>G
NM_000062.3:c.-56T>G MANE Select	NP_000053.2:n.-56T>G