Canonical Allele Identifier: CA380690842

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381995T>G (hg19) ; chr11:g.57614522T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614522T>G , CM000673.2:g.57614522T>G	GRCh38
NC_000011.9:g.57381995T>G , CM000673.1:g.57381995T>G	GRCh37
NC_000011.8:g.57138571T>G	NCBI36
NG_009625.1:g.21969T>G , LRG_105:g.21969T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1444T>G MANE Select	ENSP00000278407.4:p.Trp482Gly
ENST00000528996.2:c.*341T>G	ENSP00000431226.2:n.*341T>G
ENST00000531605.2:c.*1220T>G	ENSP00000503752.1:n.*1220T>G
ENST00000619430.2:c.1240T>G	ENSP00000478572.2:p.Trp414Gly
ENST00000676670.1:c.1444T>G	ENSP00000504807.1:p.Trp482Gly
ENST00000676741.1:n.2526T>G
ENST00000677624.1:c.*864T>G	ENSP00000503979.1:n.*864T>G
ENST00000677625.1:c.1390T>G	ENSP00000502857.1:p.Trp464Gly
ENST00000677856.1:n.1697T>G
ENST00000677915.1:c.*341T>G	ENSP00000503118.1:n.*341T>G
ENST00000678533.1:c.*998T>G	ENSP00000503873.1:n.*998T>G
ENST00000678592.1:c.*384T>G	ENSP00000504424.1:n.*384T>G
ENST00000278407.8:c.1444T>G	ENSP00000278407.4:p.Trp482Gly
ENST00000340687.10:c.1333T>G	ENSP00000341861.6:p.Trp445Gly
ENST00000378323.8:c.1459T>G	ENSP00000367574.4:p.Trp487Gly
ENST00000378324.6:c.1288T>G	ENSP00000367575.2:p.Trp430Gly
ENST00000403558.1:c.1573T>G	ENSP00000384420.1:p.Trp525Gly
ENST00000528996.1:c.645T>G	ENSP00000431226.1:n.645T>G
ENST00000530113.1:n.901T>G
ENST00000531133.5:c.945T>G	ENSP00000435431.1:n.945T>G
ENST00000531797.5:c.*469T>G	ENSP00000432554.1:n.*469T>G
ENST00000619430.1:c.575T>G	ENSP00000478572.1:n.575T>G
NM_000062.2:c.1444T>G , LRG_105t1:c.1444T>G	NP_000053.2:p.Trp482Gly
NM_001032295.1:c.1444T>G	NP_001027466.1:p.Trp482Gly
NM_000062.3:c.1444T>G MANE Select	NP_000053.2:p.Trp482Gly
NM_001032295.2:c.1444T>G	NP_001027466.1:p.Trp482Gly