Canonical Allele Identifier: CA380690241
Community Standard Title: NM_000062.3(SERPING1):c.1269T>A (p.Tyr423Ter)
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57614347T>A , CM000673.2:g.57614347T>A GRCh38
NC_000011.9:g.57381820T>A , CM000673.1:g.57381820T>A GRCh37
NC_000011.8:g.57138396T>A NCBI36
NG_009625.1:g.21794T>A , LRG_105:g.21794T>A

Transcript Alleles

HGVS Amino-acid Change
NM_000062.3:c.1269T>A MANE Select NP_000053.2:p.Tyr423Ter
ENST00000278407.9:c.1269T>A MANE Select ENSP00000278407.4:p.Tyr423Ter
NM_000062.2:c.1269T>A , LRG_105t1:c.1269T>A NP_000053.2:p.Tyr423Ter
NM_001032295.1:c.1269T>A NP_001027466.1:p.Tyr423Ter
NM_001032295.2:c.1269T>A NP_001027466.1:p.Tyr423Ter
ENST00000278407.8:c.1269T>A ENSP00000278407.4:p.Tyr423Ter
ENST00000340687.10:c.1158T>A ENSP00000341861.6:p.Tyr386Ter
ENST00000378323.8:c.1284T>A ENSP00000367574.4:p.Tyr428Ter
ENST00000378324.6:c.1113T>A ENSP00000367575.2:p.Tyr371Ter
ENST00000403558.1:c.1398T>A ENSP00000384420.1:p.Tyr466Ter
ENST00000528996.1:c.470T>A ENSP00000431226.1:n.470T>A
ENST00000528996.2:c.*166T>A ENSP00000431226.2:n.*166T>A
ENST00000530113.1:n.726T>A
ENST00000531133.5:c.770T>A ENSP00000435431.1:n.770T>A
ENST00000531605.2:c.*1045T>A ENSP00000503752.1:n.*1045T>A
ENST00000531797.5:c.*294T>A ENSP00000432554.1:n.*294T>A
ENST00000619430.1:c.400T>A ENSP00000478572.1:p.Ter134Arg
ENST00000619430.2:c.1065T>A ENSP00000478572.2:p.Tyr355Ter
ENST00000676670.1:c.1269T>A ENSP00000504807.1:p.Tyr423Ter
ENST00000676741.1:n.2351T>A
ENST00000677624.1:c.*689T>A ENSP00000503979.1:n.*689T>A
ENST00000677625.1:c.1215T>A ENSP00000502857.1:p.Tyr405Ter
ENST00000677856.1:n.1522T>A
ENST00000677915.1:c.*166T>A ENSP00000503118.1:n.*166T>A
ENST00000678533.1:c.*823T>A ENSP00000503873.1:n.*823T>A
ENST00000678592.1:c.*209T>A ENSP00000504424.1:n.*209T>A