Canonical Allele Identifier: CA6008281

Gene: SERPING1

Linked Data

• ClinVar Variation Id: 2181612
• ClinVar RCV Id: RCV002606235
• dbSNP Id: rs745853278
• ExAC: 11:57381919 G / A
• gnomAD v2: 11-57381919-G-A
• gnomAD v3: 11-57614446-G-A
• gnomAD v4: 11-57614446-G-A
• MyVariant Identifiers: chr11:g.57381919G>A (hg19) ; chr11:g.57614446G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614446G>A , CM000673.2:g.57614446G>A	GRCh38
NC_000011.9:g.57381919G>A , CM000673.1:g.57381919G>A	GRCh37
NC_000011.8:g.57138495G>A	NCBI36
NG_009625.1:g.21893G>A , LRG_105:g.21893G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1368G>A MANE Select	ENSP00000278407.4:p.Ala456=
ENST00000528996.2:c.*265G>A	ENSP00000431226.2:n.*265G>A
ENST00000531605.2:c.*1144G>A	ENSP00000503752.1:n.*1144G>A
ENST00000619430.2:c.1164G>A	ENSP00000478572.2:p.Ala388=
ENST00000676670.1:c.1368G>A	ENSP00000504807.1:p.Ala456=
ENST00000676741.1:n.2450G>A
ENST00000677624.1:c.*788G>A	ENSP00000503979.1:n.*788G>A
ENST00000677625.1:c.1314G>A	ENSP00000502857.1:p.Ala438=
ENST00000677856.1:n.1621G>A
ENST00000677915.1:c.*265G>A	ENSP00000503118.1:n.*265G>A
ENST00000678533.1:c.*922G>A	ENSP00000503873.1:n.*922G>A
ENST00000678592.1:c.*308G>A	ENSP00000504424.1:n.*308G>A
ENST00000278407.8:c.1368G>A	ENSP00000278407.4:p.Ala456=
ENST00000340687.10:c.1257G>A	ENSP00000341861.6:p.Ala419=
ENST00000378323.8:c.1383G>A	ENSP00000367574.4:p.Ala461=
ENST00000378324.6:c.1212G>A	ENSP00000367575.2:p.Ala404=
ENST00000403558.1:c.1497G>A	ENSP00000384420.1:p.Ala499=
ENST00000528996.1:c.569G>A	ENSP00000431226.1:n.569G>A
ENST00000530113.1:n.825G>A
ENST00000531133.5:c.869G>A	ENSP00000435431.1:n.869G>A
ENST00000531797.5:c.*393G>A	ENSP00000432554.1:n.*393G>A
ENST00000619430.1:c.499G>A	ENSP00000478572.1:n.499G>A
NM_000062.2:c.1368G>A , LRG_105t1:c.1368G>A	NP_000053.2:p.Ala456=
NM_001032295.1:c.1368G>A	NP_001027466.1:p.Ala456=
NM_000062.3:c.1368G>A MANE Select	NP_000053.2:p.Ala456=
NM_001032295.2:c.1368G>A	NP_001027466.1:p.Ala456=