Canonical Allele Identifier: CA2695214278

Gene: SERPING1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614517del , CM000673.2:g.57614517del	GRCh38
NC_000011.9:g.57381990del , CM000673.1:g.57381990del	GRCh37
NC_000011.8:g.57138566del	NCBI36
NG_009625.1:g.21964del , LRG_105:g.21964del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1439del MANE Select	ENSP00000278407.4:p.Val480GlyfsTer?
ENST00000528996.2:c.*336del	ENSP00000431226.2:n.*336del
ENST00000531605.2:c.*1215del	ENSP00000503752.1:n.*1215del
ENST00000619430.2:c.1235del	ENSP00000478572.2:p.Val412GlyfsTer?
ENST00000676670.1:c.1439del	ENSP00000504807.1:p.Val480GlyfsTer?
ENST00000676741.1:n.2521del
ENST00000677624.1:c.*859del	ENSP00000503979.1:n.*859del
ENST00000677625.1:c.1385del	ENSP00000502857.1:p.Val462GlyfsTer?
ENST00000677856.1:n.1692del
ENST00000677915.1:c.*336del	ENSP00000503118.1:n.*336del
ENST00000678533.1:c.*993del	ENSP00000503873.1:n.*993del
ENST00000678592.1:c.*379del	ENSP00000504424.1:n.*379del
ENST00000278407.8:c.1439del	ENSP00000278407.4:p.Val480GlyfsTer?
ENST00000340687.10:c.1328del	ENSP00000341861.6:p.Val443GlyfsTer?
ENST00000378323.8:c.1454del	ENSP00000367574.4:p.Val485GlyfsTer?
ENST00000378324.6:c.1283del	ENSP00000367575.2:p.Val428GlyfsTer?
ENST00000403558.1:c.1568del	ENSP00000384420.1:p.Val523GlyfsTer?
ENST00000528996.1:c.640del	ENSP00000431226.1:n.640del
ENST00000530113.1:n.896del
ENST00000531133.5:c.940del	ENSP00000435431.1:n.940del
ENST00000531797.5:c.*464del	ENSP00000432554.1:n.*464del
ENST00000619430.1:c.570del	ENSP00000478572.1:n.570del
NM_000062.2:c.1439del , LRG_105t1:c.1439del	NP_000053.2:p.Val480GlyfsTer?
NM_001032295.1:c.1439del	NP_001027466.1:p.Val480GlyfsTer?
NM_000062.3:c.1439del MANE Select	NP_000053.2:p.Val480GlyfsTer?
NM_001032295.2:c.1439del	NP_001027466.1:p.Val480GlyfsTer?