Canonical Allele Identifier: CA2613601102

Gene: SERPING1

Linked Data

• gnomAD v4: 11-57600106-GCCCACCACCCAA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57600114_57600125del , CM000673.2:g.57600114_57600125del	GRCh38
NC_000011.9:g.57367587_57367598del , CM000673.1:g.57367587_57367598del	GRCh37
NC_000011.8:g.57124163_57124174del	NCBI36
NG_009625.1:g.7561_7572del , LRG_105:g.7561_7572del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.287_298del MANE Select	ENSP00000278407.4:p.Thr96_Thr99del
ENST00000528996.2:c.58+1786_58+1797del	ENSP00000431226.2:n.58+1786_58+1797del
ENST00000531605.2:c.51+1793_51+1804del	ENSP00000503752.1:n.51+1793_51+1804del
ENST00000619430.2:c.287_298del	ENSP00000478572.2:p.Thr96_Thr99del
ENST00000676670.1:c.287_298del	ENSP00000504807.1:p.Thr96_Thr99del
ENST00000676741.1:n.1369_1380del
ENST00000677275.1:n.274_285del
ENST00000677624.1:c.287_298del	ENSP00000503979.1:p.Thr96_Thr99del
ENST00000677625.1:c.287_298del	ENSP00000502857.1:p.Thr96_Thr99del
ENST00000677856.1:n.346_357del
ENST00000677915.1:c.287_298del	ENSP00000503118.1:p.Thr96_Thr99del
ENST00000678533.1:c.51+1793_51+1804del	ENSP00000503873.1:n.51+1793_51+1804del
ENST00000678592.1:c.287_298del	ENSP00000504424.1:p.Thr96_Thr99del
ENST00000278407.8:c.287_298del	ENSP00000278407.4:p.Thr96_Thr99del
ENST00000340687.10:c.287_298del	ENSP00000341861.6:p.Thr96_Thr99del
ENST00000378323.8:c.302_313del	ENSP00000367574.4:p.Thr101_Thr104del
ENST00000378324.6:c.131_142del	ENSP00000367575.2:p.Thr44_Thr47del
ENST00000403558.1:c.389_400del	ENSP00000384420.1:p.Thr130_Thr133del
ENST00000405496.5:c.287_298del	ENSP00000384561.1:p.Thr96_Thr99del
ENST00000531133.5:c.51+1793_51+1804del	ENSP00000435431.1:n.51+1793_51+1804del
ENST00000531797.5:c.51+1793_51+1804del	ENSP00000432554.1:n.51+1793_51+1804del
ENST00000619430.1:c.287_298del	ENSP00000478572.1:p.Thr96_Thr99del
NM_000062.2:c.287_298del , LRG_105t1:c.287_298del	NP_000053.2:p.Thr96_Thr99del
NM_001032295.1:c.287_298del	NP_001027466.1:p.Thr96_Thr99del
NM_000062.3:c.287_298del MANE Select	NP_000053.2:p.Thr96_Thr99del
NM_001032295.2:c.287_298del	NP_001027466.1:p.Thr96_Thr99del