Canonical Allele Identifier: CA380690855

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57382000C>A (hg19) ; chr11:g.57614527C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614527C>A , CM000673.2:g.57614527C>A	GRCh38
NC_000011.9:g.57382000C>A , CM000673.1:g.57382000C>A	GRCh37
NC_000011.8:g.57138576C>A	NCBI36
NG_009625.1:g.21974C>A , LRG_105:g.21974C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1449C>A MANE Select	ENSP00000278407.4:p.Asp483Glu
ENST00000528996.2:c.*346C>A	ENSP00000431226.2:n.*346C>A
ENST00000531605.2:c.*1225C>A	ENSP00000503752.1:n.*1225C>A
ENST00000619430.2:c.1245C>A	ENSP00000478572.2:p.Asp415Glu
ENST00000676670.1:c.1449C>A	ENSP00000504807.1:p.Asp483Glu
ENST00000676741.1:n.2531C>A
ENST00000677624.1:c.*869C>A	ENSP00000503979.1:n.*869C>A
ENST00000677625.1:c.1395C>A	ENSP00000502857.1:p.Asp465Glu
ENST00000677856.1:n.1702C>A
ENST00000677915.1:c.*346C>A	ENSP00000503118.1:n.*346C>A
ENST00000678533.1:c.*1003C>A	ENSP00000503873.1:n.*1003C>A
ENST00000678592.1:c.*389C>A	ENSP00000504424.1:n.*389C>A
ENST00000278407.8:c.1449C>A	ENSP00000278407.4:p.Asp483Glu
ENST00000340687.10:c.1338C>A	ENSP00000341861.6:p.Asp446Glu
ENST00000378323.8:c.1464C>A	ENSP00000367574.4:p.Asp488Glu
ENST00000378324.6:c.1293C>A	ENSP00000367575.2:p.Asp431Glu
ENST00000403558.1:c.1578C>A	ENSP00000384420.1:p.Asp526Glu
ENST00000528996.1:c.650C>A	ENSP00000431226.1:n.650C>A
ENST00000530113.1:n.906C>A
ENST00000531133.5:c.950C>A	ENSP00000435431.1:n.950C>A
ENST00000531797.5:c.*474C>A	ENSP00000432554.1:n.*474C>A
ENST00000619430.1:c.580C>A	ENSP00000478572.1:n.580C>A
NM_000062.2:c.1449C>A , LRG_105t1:c.1449C>A	NP_000053.2:p.Asp483Glu
NM_001032295.1:c.1449C>A	NP_001027466.1:p.Asp483Glu
NM_000062.3:c.1449C>A MANE Select	NP_000053.2:p.Asp483Glu
NM_001032295.2:c.1449C>A	NP_001027466.1:p.Asp483Glu