Canonical Allele Identifier: CA380690635

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381903A>G (hg19) ; chr11:g.57614430A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614430A>G , CM000673.2:g.57614430A>G	GRCh38
NC_000011.9:g.57381903A>G , CM000673.1:g.57381903A>G	GRCh37
NC_000011.8:g.57138479A>G	NCBI36
NG_009625.1:g.21877A>G , LRG_105:g.21877A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1352A>G MANE Select	ENSP00000278407.4:p.Glu451Gly
ENST00000528996.2:c.*249A>G	ENSP00000431226.2:n.*249A>G
ENST00000531605.2:c.*1128A>G	ENSP00000503752.1:n.*1128A>G
ENST00000619430.2:c.1148A>G	ENSP00000478572.2:p.Glu383Gly
ENST00000676670.1:c.1352A>G	ENSP00000504807.1:p.Glu451Gly
ENST00000676741.1:n.2434A>G
ENST00000677624.1:c.*772A>G	ENSP00000503979.1:n.*772A>G
ENST00000677625.1:c.1298A>G	ENSP00000502857.1:p.Glu433Gly
ENST00000677856.1:n.1605A>G
ENST00000677915.1:c.*249A>G	ENSP00000503118.1:n.*249A>G
ENST00000678533.1:c.*906A>G	ENSP00000503873.1:n.*906A>G
ENST00000678592.1:c.*292A>G	ENSP00000504424.1:n.*292A>G
ENST00000278407.8:c.1352A>G	ENSP00000278407.4:p.Glu451Gly
ENST00000340687.10:c.1241A>G	ENSP00000341861.6:p.Glu414Gly
ENST00000378323.8:c.1367A>G	ENSP00000367574.4:p.Glu456Gly
ENST00000378324.6:c.1196A>G	ENSP00000367575.2:p.Glu399Gly
ENST00000403558.1:c.1481A>G	ENSP00000384420.1:p.Glu494Gly
ENST00000528996.1:c.553A>G	ENSP00000431226.1:n.553A>G
ENST00000530113.1:n.809A>G
ENST00000531133.5:c.853A>G	ENSP00000435431.1:n.853A>G
ENST00000531797.5:c.*377A>G	ENSP00000432554.1:n.*377A>G
ENST00000619430.1:c.483A>G	ENSP00000478572.1:n.483A>G
NM_000062.2:c.1352A>G , LRG_105t1:c.1352A>G	NP_000053.2:p.Glu451Gly
NM_001032295.1:c.1352A>G	NP_001027466.1:p.Glu451Gly
NM_000062.3:c.1352A>G MANE Select	NP_000053.2:p.Glu451Gly
NM_001032295.2:c.1352A>G	NP_001027466.1:p.Glu451Gly