Canonical Allele Identifier: CA380690162

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381811T>A (hg19) ; chr11:g.57614338T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614338T>A , CM000673.2:g.57614338T>A	GRCh38
NC_000011.9:g.57381811T>A , CM000673.1:g.57381811T>A	GRCh37
NC_000011.8:g.57138387T>A	NCBI36
NG_009625.1:g.21785T>A , LRG_105:g.21785T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1260T>A MANE Select	ENSP00000278407.4:p.Asp420Glu
ENST00000528996.2:c.*157T>A	ENSP00000431226.2:n.*157T>A
ENST00000531605.2:c.*1036T>A	ENSP00000503752.1:n.*1036T>A
ENST00000619430.2:c.1056T>A	ENSP00000478572.2:p.Asp352Glu
ENST00000676670.1:c.1260T>A	ENSP00000504807.1:p.Asp420Glu
ENST00000676741.1:n.2342T>A
ENST00000677624.1:c.*680T>A	ENSP00000503979.1:n.*680T>A
ENST00000677625.1:c.1206T>A	ENSP00000502857.1:p.Asp402Glu
ENST00000677856.1:n.1513T>A
ENST00000677915.1:c.*157T>A	ENSP00000503118.1:n.*157T>A
ENST00000678533.1:c.*814T>A	ENSP00000503873.1:n.*814T>A
ENST00000678592.1:c.*200T>A	ENSP00000504424.1:n.*200T>A
ENST00000278407.8:c.1260T>A	ENSP00000278407.4:p.Asp420Glu
ENST00000340687.10:c.1149T>A	ENSP00000341861.6:p.Asp383Glu
ENST00000378323.8:c.1275T>A	ENSP00000367574.4:p.Asp425Glu
ENST00000378324.6:c.1104T>A	ENSP00000367575.2:p.Asp368Glu
ENST00000403558.1:c.1389T>A	ENSP00000384420.1:p.Asp463Glu
ENST00000528996.1:c.461T>A	ENSP00000431226.1:n.461T>A
ENST00000530113.1:n.717T>A
ENST00000531133.5:c.761T>A	ENSP00000435431.1:n.761T>A
ENST00000531797.5:c.*285T>A	ENSP00000432554.1:n.*285T>A
ENST00000619430.1:c.391T>A	ENSP00000478572.1:p.Phe131Ile
NM_000062.2:c.1260T>A , LRG_105t1:c.1260T>A	NP_000053.2:p.Asp420Glu
NM_001032295.1:c.1260T>A	NP_001027466.1:p.Asp420Glu
NM_000062.3:c.1260T>A MANE Select	NP_000053.2:p.Asp420Glu
NM_001032295.2:c.1260T>A	NP_001027466.1:p.Asp420Glu