Canonical Allele Identifier: CA6008273

Gene: SERPING1

Linked Data

• dbSNP Id: rs755491309
• ExAC: 11:57381844 A / G
• gnomAD v2: 11-57381844-A-G
• gnomAD v4: 11-57614371-A-G
• MyVariant Identifiers: chr11:g.57381844A>G (hg19) ; chr11:g.57614371A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614371A>G , CM000673.2:g.57614371A>G	GRCh38
NC_000011.9:g.57381844A>G , CM000673.1:g.57381844A>G	GRCh37
NC_000011.8:g.57138420A>G	NCBI36
NG_009625.1:g.21818A>G , LRG_105:g.21818A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.1293A>G MANE Select	ENSP00000278407.4:p.Thr431=
ENST00000528996.2:c.*190A>G	ENSP00000431226.2:n.*190A>G
ENST00000531605.2:c.*1069A>G	ENSP00000503752.1:n.*1069A>G
ENST00000619430.2:c.1089A>G	ENSP00000478572.2:p.Thr363=
ENST00000676670.1:c.1293A>G	ENSP00000504807.1:p.Thr431=
ENST00000676741.1:n.2375A>G
ENST00000677624.1:c.*713A>G	ENSP00000503979.1:n.*713A>G
ENST00000677625.1:c.1239A>G	ENSP00000502857.1:p.Thr413=
ENST00000677856.1:n.1546A>G
ENST00000677915.1:c.*190A>G	ENSP00000503118.1:n.*190A>G
ENST00000678533.1:c.*847A>G	ENSP00000503873.1:n.*847A>G
ENST00000678592.1:c.*233A>G	ENSP00000504424.1:n.*233A>G
ENST00000278407.8:c.1293A>G	ENSP00000278407.4:p.Thr431=
ENST00000340687.10:c.1182A>G	ENSP00000341861.6:p.Thr394=
ENST00000378323.8:c.1308A>G	ENSP00000367574.4:p.Thr436=
ENST00000378324.6:c.1137A>G	ENSP00000367575.2:p.Thr379=
ENST00000403558.1:c.1422A>G	ENSP00000384420.1:p.Thr474=
ENST00000528996.1:c.494A>G	ENSP00000431226.1:n.494A>G
ENST00000530113.1:n.750A>G
ENST00000531133.5:c.794A>G	ENSP00000435431.1:n.794A>G
ENST00000531797.5:c.*318A>G	ENSP00000432554.1:n.*318A>G
ENST00000619430.1:c.424A>G	ENSP00000478572.1:n.424A>G
NM_000062.2:c.1293A>G , LRG_105t1:c.1293A>G	NP_000053.2:p.Thr431=
NM_001032295.1:c.1293A>G	NP_001027466.1:p.Thr431=
NM_000062.3:c.1293A>G MANE Select	NP_000053.2:p.Thr431=
NM_001032295.2:c.1293A>G	NP_001027466.1:p.Thr431=