Canonical Allele Identifier: CA219263

Gene: SERPING1

Linked Data

• ClinVar Variation Id: 68251
• ClinVar RCV Id: RCV000059089
• dbSNP Id: rs281875168
• COSMIC: COSM1298212
• MyVariant Identifiers: chr11:g.57367761A>G (hg19) ; chr11:g.57600288A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57600288A>G , CM000673.2:g.57600288A>G	GRCh38
NC_000011.9:g.57367761A>G , CM000673.1:g.57367761A>G	GRCh37
NC_000011.8:g.57124337A>G	NCBI36
NG_009625.1:g.7735A>G , LRG_105:g.7735A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.461A>G MANE Select	ENSP00000278407.4:p.Tyr154Cys
ENST00000528996.2:c.58+1960A>G	ENSP00000431226.2:n.58+1960A>G
ENST00000531605.2:c.52-1747A>G	ENSP00000503752.1:n.52-1747A>G
ENST00000619430.2:c.461A>G	ENSP00000478572.2:p.Tyr154Cys
ENST00000676670.1:c.461A>G	ENSP00000504807.1:p.Tyr154Cys
ENST00000676741.1:n.1543A>G
ENST00000677275.1:n.448A>G
ENST00000677624.1:c.461A>G	ENSP00000503979.1:p.Tyr154Cys
ENST00000677625.1:c.461A>G	ENSP00000502857.1:p.Tyr154Cys
ENST00000677856.1:n.520A>G
ENST00000677915.1:c.461A>G	ENSP00000503118.1:p.Tyr154Cys
ENST00000678533.1:c.52-1747A>G	ENSP00000503873.1:n.52-1747A>G
ENST00000678592.1:c.461A>G	ENSP00000504424.1:p.Tyr154Cys
ENST00000278407.8:c.461A>G	ENSP00000278407.4:p.Tyr154Cys
ENST00000340687.10:c.461A>G	ENSP00000341861.6:p.Tyr154Cys
ENST00000378323.8:c.476A>G	ENSP00000367574.4:p.Tyr159Cys
ENST00000378324.6:c.305A>G	ENSP00000367575.2:p.Tyr102Cys
ENST00000403558.1:c.563A>G	ENSP00000384420.1:p.Tyr188Cys
ENST00000405496.5:c.461A>G	ENSP00000384561.1:p.Tyr154Cys
ENST00000531133.5:c.52-1747A>G	ENSP00000435431.1:n.52-1747A>G
ENST00000531797.5:c.52-1747A>G	ENSP00000432554.1:n.52-1747A>G
ENST00000619430.1:c.348+113A>G	ENSP00000478572.1:n.348+113A>G
NM_000062.2:c.461A>G , LRG_105t1:c.461A>G	NP_000053.2:p.Tyr154Cys
NM_001032295.1:c.461A>G	NP_001027466.1:p.Tyr154Cys
NM_000062.3:c.461A>G MANE Select	NP_000053.2:p.Tyr154Cys
NM_001032295.2:c.461A>G	NP_001027466.1:p.Tyr154Cys