Canonical Allele Identifier: CA380694195

Gene: SERPING1

Linked Data

• ClinVar Variation Id: 619175
• ClinVar RCV Id: RCV000758137
• dbSNP Id: rs1565169419
• MyVariant Identifiers: chr11:g.57367355A>T (hg19) ; chr11:g.57599882A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57599882A>T , CM000673.2:g.57599882A>T	GRCh38
NC_000011.9:g.57367355A>T , CM000673.1:g.57367355A>T	GRCh37
NC_000011.8:g.57123931A>T	NCBI36
NG_009625.1:g.7329A>T , LRG_105:g.7329A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.55A>T MANE Select	ENSP00000278407.4:p.Arg19Ter
ENST00000528996.2:c.58+1554A>T	ENSP00000431226.2:n.58+1554A>T
ENST00000531605.2:c.51+1561A>T	ENSP00000503752.1:n.51+1561A>T
ENST00000619430.2:c.55A>T	ENSP00000478572.2:p.Arg19Ter
ENST00000676670.1:c.55A>T	ENSP00000504807.1:p.Arg19Ter
ENST00000676741.1:n.1137A>T
ENST00000677275.1:n.42A>T
ENST00000677624.1:c.55A>T	ENSP00000503979.1:p.Arg19Ter
ENST00000677625.1:c.55A>T	ENSP00000502857.1:p.Arg19Ter
ENST00000677856.1:n.114A>T
ENST00000677915.1:c.55A>T	ENSP00000503118.1:p.Arg19Ter
ENST00000678533.1:c.51+1561A>T	ENSP00000503873.1:n.51+1561A>T
ENST00000678592.1:c.55A>T	ENSP00000504424.1:p.Arg19Ter
ENST00000278407.8:c.55A>T	ENSP00000278407.4:p.Arg19Ter
ENST00000340687.10:c.55A>T	ENSP00000341861.6:p.Arg19Ter
ENST00000378323.8:c.70A>T	ENSP00000367574.4:p.Arg24Ter
ENST00000378324.6:c.-102A>T	ENSP00000367575.2:n.-102A>T
ENST00000403558.1:c.157A>T	ENSP00000384420.1:p.Arg53Ter
ENST00000405496.5:c.55A>T	ENSP00000384561.1:p.Arg19Ter
ENST00000457869.1:c.157A>T	ENSP00000399746.1:p.Arg53Ter
ENST00000531133.5:c.51+1561A>T	ENSP00000435431.1:n.51+1561A>T
ENST00000531797.5:c.51+1561A>T	ENSP00000432554.1:n.51+1561A>T
ENST00000619430.1:c.55A>T	ENSP00000478572.1:p.Arg19Ter
NM_000062.2:c.55A>T , LRG_105t1:c.55A>T	NP_000053.2:p.Arg19Ter
NM_001032295.1:c.55A>T	NP_001027466.1:p.Arg19Ter
NM_000062.3:c.55A>T MANE Select	NP_000053.2:p.Arg19Ter
NM_001032295.2:c.55A>T	NP_001027466.1:p.Arg19Ter