Canonical Allele Identifier: CA1975538938

Gene: SERPING1

Linked Data

• dbSNP Id: rs998665831
• gnomAD v4: 11-57614255-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614255C>G , CM000673.2:g.57614255C>G	GRCh38
NC_000011.9:g.57381728C>G , CM000673.1:g.57381728C>G	GRCh37
NC_000011.8:g.57138304C>G	NCBI36
NG_009625.1:g.21702C>G , LRG_105:g.21702C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1250-73C>G MANE Select	ENSP00000278407.4:n.1250-73C>G
ENST00000528996.2:c.*147-73C>G	ENSP00000431226.2:n.*147-73C>G
ENST00000531605.2:c.*1026-73C>G	ENSP00000503752.1:n.*1026-73C>G
ENST00000619430.2:c.1046-73C>G	ENSP00000478572.2:n.1046-73C>G
ENST00000676670.1:c.1250-73C>G	ENSP00000504807.1:n.1250-73C>G
ENST00000676741.1:n.2332-73C>G
ENST00000677624.1:c.*670-73C>G	ENSP00000503979.1:n.*670-73C>G
ENST00000677625.1:c.1196-73C>G	ENSP00000502857.1:n.1196-73C>G
ENST00000677856.1:n.1503-73C>G
ENST00000677915.1:c.*147-73C>G	ENSP00000503118.1:n.*147-73C>G
ENST00000678533.1:c.*804-73C>G	ENSP00000503873.1:n.*804-73C>G
ENST00000678592.1:c.*190-73C>G	ENSP00000504424.1:n.*190-73C>G
ENST00000278407.8:c.1250-73C>G	ENSP00000278407.4:n.1250-73C>G
ENST00000340687.10:c.1139-73C>G	ENSP00000341861.6:n.1139-73C>G
ENST00000378323.8:c.1265-73C>G	ENSP00000367574.4:n.1265-73C>G
ENST00000378324.6:c.1094-73C>G	ENSP00000367575.2:n.1094-73C>G
ENST00000403558.1:c.1379-73C>G	ENSP00000384420.1:n.1379-73C>G
ENST00000528996.1:c.451-73C>G	ENSP00000431226.1:n.451-73C>G
ENST00000530113.1:n.707-73C>G
ENST00000531133.5:c.751-73C>G	ENSP00000435431.1:n.751-73C>G
ENST00000531797.5:c.*275-73C>G	ENSP00000432554.1:n.*275-73C>G
ENST00000619430.1:c.381-73C>G	ENSP00000478572.1:n.381-73C>G
NM_000062.2:c.1250-73C>G , LRG_105t1:c.1250-73C>G	NP_000053.2:n.1250-73C>G
NM_001032295.1:c.1250-73C>G	NP_001027466.1:n.1250-73C>G
NM_000062.3:c.1250-73C>G MANE Select	NP_000053.2:n.1250-73C>G
NM_001032295.2:c.1250-73C>G	NP_001027466.1:n.1250-73C>G