Canonical Allele Identifier: CA380690705

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381927C>G (hg19) ; chr11:g.57614454C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614454C>G , CM000673.2:g.57614454C>G	GRCh38
NC_000011.9:g.57381927C>G , CM000673.1:g.57381927C>G	GRCh37
NC_000011.8:g.57138503C>G	NCBI36
NG_009625.1:g.21901C>G , LRG_105:g.21901C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1376C>G MANE Select	ENSP00000278407.4:p.Ala459Gly
ENST00000528996.2:c.*273C>G	ENSP00000431226.2:n.*273C>G
ENST00000531605.2:c.*1152C>G	ENSP00000503752.1:n.*1152C>G
ENST00000619430.2:c.1172C>G	ENSP00000478572.2:p.Ala391Gly
ENST00000676670.1:c.1376C>G	ENSP00000504807.1:p.Ala459Gly
ENST00000676741.1:n.2458C>G
ENST00000677624.1:c.*796C>G	ENSP00000503979.1:n.*796C>G
ENST00000677625.1:c.1322C>G	ENSP00000502857.1:p.Ala441Gly
ENST00000677856.1:n.1629C>G
ENST00000677915.1:c.*273C>G	ENSP00000503118.1:n.*273C>G
ENST00000678533.1:c.*930C>G	ENSP00000503873.1:n.*930C>G
ENST00000678592.1:c.*316C>G	ENSP00000504424.1:n.*316C>G
ENST00000278407.8:c.1376C>G	ENSP00000278407.4:p.Ala459Gly
ENST00000340687.10:c.1265C>G	ENSP00000341861.6:p.Ala422Gly
ENST00000378323.8:c.1391C>G	ENSP00000367574.4:p.Ala464Gly
ENST00000378324.6:c.1220C>G	ENSP00000367575.2:p.Ala407Gly
ENST00000403558.1:c.1505C>G	ENSP00000384420.1:p.Ala502Gly
ENST00000528996.1:c.577C>G	ENSP00000431226.1:n.577C>G
ENST00000530113.1:n.833C>G
ENST00000531133.5:c.877C>G	ENSP00000435431.1:n.877C>G
ENST00000531797.5:c.*401C>G	ENSP00000432554.1:n.*401C>G
ENST00000619430.1:c.507C>G	ENSP00000478572.1:n.507C>G
NM_000062.2:c.1376C>G , LRG_105t1:c.1376C>G	NP_000053.2:p.Ala459Gly
NM_001032295.1:c.1376C>G	NP_001027466.1:p.Ala459Gly
NM_000062.3:c.1376C>G MANE Select	NP_000053.2:p.Ala459Gly
NM_001032295.2:c.1376C>G	NP_001027466.1:p.Ala459Gly