Canonical Allele Identifier: CA380690846
Community Standard Title: NM_000062.3(SERPING1):c.1446G>A (p.Trp482Ter)
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57614524G>A , CM000673.2:g.57614524G>A GRCh38
NC_000011.9:g.57381997G>A , CM000673.1:g.57381997G>A GRCh37
NC_000011.8:g.57138573G>A NCBI36
NG_009625.1:g.21971G>A , LRG_105:g.21971G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000062.3:c.1446G>A MANE Select NP_000053.2:p.Trp482Ter
ENST00000278407.9:c.1446G>A MANE Select ENSP00000278407.4:p.Trp482Ter
NM_000062.2:c.1446G>A , LRG_105t1:c.1446G>A NP_000053.2:p.Trp482Ter
NM_001032295.1:c.1446G>A NP_001027466.1:p.Trp482Ter
NM_001032295.2:c.1446G>A NP_001027466.1:p.Trp482Ter
ENST00000278407.8:c.1446G>A ENSP00000278407.4:p.Trp482Ter
ENST00000340687.10:c.1335G>A ENSP00000341861.6:p.Trp445Ter
ENST00000378323.8:c.1461G>A ENSP00000367574.4:p.Trp487Ter
ENST00000378324.6:c.1290G>A ENSP00000367575.2:p.Trp430Ter
ENST00000403558.1:c.1575G>A ENSP00000384420.1:p.Trp525Ter
ENST00000528996.1:c.647G>A ENSP00000431226.1:n.647G>A
ENST00000528996.2:c.*343G>A ENSP00000431226.2:n.*343G>A
ENST00000530113.1:n.903G>A
ENST00000531133.5:c.947G>A ENSP00000435431.1:n.947G>A
ENST00000531605.2:c.*1222G>A ENSP00000503752.1:n.*1222G>A
ENST00000531797.5:c.*471G>A ENSP00000432554.1:n.*471G>A
ENST00000619430.1:c.577G>A ENSP00000478572.1:n.577G>A
ENST00000619430.2:c.1242G>A ENSP00000478572.2:p.Trp414Ter
ENST00000676670.1:c.1446G>A ENSP00000504807.1:p.Trp482Ter
ENST00000676741.1:n.2528G>A
ENST00000677624.1:c.*866G>A ENSP00000503979.1:n.*866G>A
ENST00000677625.1:c.1392G>A ENSP00000502857.1:p.Trp464Ter
ENST00000677856.1:n.1699G>A
ENST00000677915.1:c.*343G>A ENSP00000503118.1:n.*343G>A
ENST00000678533.1:c.*1000G>A ENSP00000503873.1:n.*1000G>A
ENST00000678592.1:c.*386G>A ENSP00000504424.1:n.*386G>A