Canonical Allele Identifier: CA2613603556

Gene: SERPING1

Linked Data

• gnomAD v4: 11-57614641-C-CAGG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614641_57614642insAGG , CM000673.2:g.57614641_57614642insAGG	GRCh38
NC_000011.9:g.57382114_57382115insAGG , CM000673.1:g.57382114_57382115insAGG	GRCh37
NC_000011.8:g.57138690_57138691insAGG	NCBI36
NG_009625.1:g.22088_22089insAGG , LRG_105:g.22088_22089insAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.*60_*61insAGG MANE Select	ENSP00000278407.4:n.*60_*61insAGG
ENST00000528996.2:c.*460_*461insAGG	ENSP00000431226.2:n.*460_*461insAGG
ENST00000531605.2:c.*1339_*1340insAGG	ENSP00000503752.1:n.*1339_*1340insAGG
ENST00000619430.2:c.*60_*61insAGG	ENSP00000478572.2:n.*60_*61insAGG
ENST00000676670.1:c.*15+45_*15+46insAGG	ENSP00000504807.1:n.*15+45_*15+46insAGG
ENST00000676741.1:n.2645_2646insAGG
ENST00000677624.1:c.*983_*984insAGG	ENSP00000503979.1:n.*983_*984insAGG
ENST00000677625.1:c.*60_*61insAGG	ENSP00000502857.1:n.*60_*61insAGG
ENST00000677856.1:n.1816_1817insAGG
ENST00000677915.1:c.*460_*461insAGG	ENSP00000503118.1:n.*460_*461insAGG
ENST00000678533.1:c.*1072+45_*1072+46insAGG	ENSP00000503873.1:n.*1072+45_*1072+46insAGG
ENST00000678592.1:c.*503_*504insAGG	ENSP00000504424.1:n.*503_*504insAGG
ENST00000278407.8:c.*60_*61insAGG	ENSP00000278407.4:n.*60_*61insAGG
ENST00000340687.10:c.*60_*61insAGG	ENSP00000341861.6:n.*60_*61insAGG
ENST00000378323.8:c.*60_*61insAGG	ENSP00000367574.4:n.*60_*61insAGG
ENST00000378324.6:c.*60_*61insAGG	ENSP00000367575.2:n.*60_*61insAGG
ENST00000403558.1:c.*60_*61insAGG	ENSP00000384420.1:n.*60_*61insAGG
ENST00000528996.1:c.764_765insAGG	ENSP00000431226.1:n.764_765insAGG
ENST00000531797.5:c.*588_*589insAGG	ENSP00000432554.1:n.*588_*589insAGG
NM_000062.2:c.*60_*61insAGG , LRG_105t1:c.*60_*61insAGG	NP_000053.2:n.*60_*61insAGG
NM_001032295.1:c.*60_*61insAGG	NP_001027466.1:n.*60_*61insAGG
NM_000062.3:c.*60_*61insAGG MANE Select	NP_000053.2:n.*60_*61insAGG
NM_001032295.2:c.*60_*61insAGG	NP_001027466.1:n.*60_*61insAGG