Canonical Allele Identifier: CA474564906

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57382051C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614578C>A , CM000673.2:g.57614578C>A	GRCh38
NC_000011.9:g.57382051C>A , CM000673.1:g.57382051C>A	GRCh37
NC_000011.8:g.57138627C>A	NCBI36
NG_009625.1:g.22025C>A , LRG_105:g.22025C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1500C>A MANE Select	ENSP00000278407.4:p.Ala500=
ENST00000528996.2:c.*397C>A	ENSP00000431226.2:n.*397C>A
ENST00000531605.2:c.*1276C>A	ENSP00000503752.1:n.*1276C>A
ENST00000619430.2:c.1296C>A	ENSP00000478572.2:p.Ala432=
ENST00000676670.1:c.1500C>A	ENSP00000504807.1:p.Ala500=
ENST00000676741.1:n.2582C>A
ENST00000677624.1:c.*920C>A	ENSP00000503979.1:n.*920C>A
ENST00000677625.1:c.1446C>A	ENSP00000502857.1:p.Ala482=
ENST00000677856.1:n.1753C>A
ENST00000677915.1:c.*397C>A	ENSP00000503118.1:n.*397C>A
ENST00000678533.1:c.*1054C>A	ENSP00000503873.1:n.*1054C>A
ENST00000678592.1:c.*440C>A	ENSP00000504424.1:n.*440C>A
ENST00000278407.8:c.1500C>A	ENSP00000278407.4:p.Ala500=
ENST00000340687.10:c.1389C>A	ENSP00000341861.6:p.Ala463=
ENST00000378323.8:c.1515C>A	ENSP00000367574.4:p.Ala505=
ENST00000378324.6:c.1344C>A	ENSP00000367575.2:p.Ala448=
ENST00000403558.1:c.1629C>A	ENSP00000384420.1:p.Ala543=
ENST00000528996.1:c.701C>A	ENSP00000431226.1:n.701C>A
ENST00000531133.5:c.1001C>A	ENSP00000435431.1:n.1001C>A
ENST00000531797.5:c.*525C>A	ENSP00000432554.1:n.*525C>A
ENST00000619430.1:c.631C>A	ENSP00000478572.1:n.631C>A
NM_000062.2:c.1500C>A , LRG_105t1:c.1500C>A	NP_000053.2:p.Ala500=
NM_001032295.1:c.1500C>A	NP_001027466.1:p.Ala500=
NM_000062.3:c.1500C>A MANE Select	NP_000053.2:p.Ala500=
NM_001032295.2:c.1500C>A	NP_001027466.1:p.Ala500=