Canonical Allele Identifier: CA2613601171

Gene: SERPING1

Linked Data

• gnomAD v4: 11-57600114-C-CCCAACCCACCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57600125_57600136dup , CM000673.2:g.57600125_57600136dup	GRCh38
NC_000011.9:g.57367598_57367609dup , CM000673.1:g.57367598_57367609dup	GRCh37
NC_000011.8:g.57124174_57124185dup	NCBI36
NG_009625.1:g.7572_7583dup , LRG_105:g.7572_7583dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.298_309dup MANE Select	ENSP00000278407.4:p.Thr103_Gln104insIleGlnProThr
ENST00000528996.2:c.58+1797_58+1808dup	ENSP00000431226.2:n.58+1797_58+1808dup
ENST00000531605.2:c.51+1804_51+1815dup	ENSP00000503752.1:n.51+1804_51+1815dup
ENST00000619430.2:c.298_309dup	ENSP00000478572.2:p.Thr103_Gln104insIleGlnProThr
ENST00000676670.1:c.298_309dup	ENSP00000504807.1:p.Thr103_Gln104insIleGlnProThr
ENST00000676741.1:n.1380_1391dup
ENST00000677275.1:n.285_296dup
ENST00000677624.1:c.298_309dup	ENSP00000503979.1:p.Thr103_Gln104insIleGlnProThr
ENST00000677625.1:c.298_309dup	ENSP00000502857.1:p.Thr103_Gln104insIleGlnProThr
ENST00000677856.1:n.357_368dup
ENST00000677915.1:c.298_309dup	ENSP00000503118.1:p.Thr103_Gln104insIleGlnProThr
ENST00000678533.1:c.51+1804_51+1815dup	ENSP00000503873.1:n.51+1804_51+1815dup
ENST00000678592.1:c.298_309dup	ENSP00000504424.1:p.Thr103_Gln104insIleGlnProThr
ENST00000278407.8:c.298_309dup	ENSP00000278407.4:p.Thr103_Gln104insIleGlnProThr
ENST00000340687.10:c.298_309dup	ENSP00000341861.6:p.Thr103_Gln104insIleGlnProThr
ENST00000378323.8:c.313_324dup	ENSP00000367574.4:p.Thr108_Gln109insIleGlnProThr
ENST00000378324.6:c.142_153dup	ENSP00000367575.2:p.Thr51_Gln52insIleGlnProThr
ENST00000403558.1:c.400_411dup	ENSP00000384420.1:p.Thr137_Gln138insIleGlnProThr
ENST00000405496.5:c.298_309dup	ENSP00000384561.1:p.Thr103_Gln104insIleGlnProThr
ENST00000531133.5:c.51+1804_51+1815dup	ENSP00000435431.1:n.51+1804_51+1815dup
ENST00000531797.5:c.51+1804_51+1815dup	ENSP00000432554.1:n.51+1804_51+1815dup
ENST00000619430.1:c.298_309dup	ENSP00000478572.1:p.Thr103_Gln104insIleGlnProThr
NM_000062.2:c.298_309dup , LRG_105t1:c.298_309dup	NP_000053.2:p.Thr103_Gln104insIleGlnProThr
NM_001032295.1:c.298_309dup	NP_001027466.1:p.Thr103_Gln104insIleGlnProThr
NM_000062.3:c.298_309dup MANE Select	NP_000053.2:p.Thr103_Gln104insIleGlnProThr
NM_001032295.2:c.298_309dup	NP_001027466.1:p.Thr103_Gln104insIleGlnProThr