Canonical Allele Identifier: CA380690814

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381983C>A (hg19) ; chr11:g.57614510C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614510C>A , CM000673.2:g.57614510C>A	GRCh38
NC_000011.9:g.57381983C>A , CM000673.1:g.57381983C>A	GRCh37
NC_000011.8:g.57138559C>A	NCBI36
NG_009625.1:g.21957C>A , LRG_105:g.21957C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1432C>A MANE Select	ENSP00000278407.4:p.Leu478Ile
ENST00000528996.2:c.*329C>A	ENSP00000431226.2:n.*329C>A
ENST00000531605.2:c.*1208C>A	ENSP00000503752.1:n.*1208C>A
ENST00000619430.2:c.1228C>A	ENSP00000478572.2:p.Leu410Ile
ENST00000676670.1:c.1432C>A	ENSP00000504807.1:p.Leu478Ile
ENST00000676741.1:n.2514C>A
ENST00000677624.1:c.*852C>A	ENSP00000503979.1:n.*852C>A
ENST00000677625.1:c.1378C>A	ENSP00000502857.1:p.Leu460Ile
ENST00000677856.1:n.1685C>A
ENST00000677915.1:c.*329C>A	ENSP00000503118.1:n.*329C>A
ENST00000678533.1:c.*986C>A	ENSP00000503873.1:n.*986C>A
ENST00000678592.1:c.*372C>A	ENSP00000504424.1:n.*372C>A
ENST00000278407.8:c.1432C>A	ENSP00000278407.4:p.Leu478Ile
ENST00000340687.10:c.1321C>A	ENSP00000341861.6:p.Leu441Ile
ENST00000378323.8:c.1447C>A	ENSP00000367574.4:p.Leu483Ile
ENST00000378324.6:c.1276C>A	ENSP00000367575.2:p.Leu426Ile
ENST00000403558.1:c.1561C>A	ENSP00000384420.1:p.Leu521Ile
ENST00000528996.1:c.633C>A	ENSP00000431226.1:n.633C>A
ENST00000530113.1:n.889C>A
ENST00000531133.5:c.933C>A	ENSP00000435431.1:n.933C>A
ENST00000531797.5:c.*457C>A	ENSP00000432554.1:n.*457C>A
ENST00000619430.1:c.563C>A	ENSP00000478572.1:n.563C>A
NM_000062.2:c.1432C>A , LRG_105t1:c.1432C>A	NP_000053.2:p.Leu478Ile
NM_001032295.1:c.1432C>A	NP_001027466.1:p.Leu478Ile
NM_000062.3:c.1432C>A MANE Select	NP_000053.2:p.Leu478Ile
NM_001032295.2:c.1432C>A	NP_001027466.1:p.Leu478Ile