Canonical Allele Identifier: CA380690711

Gene: SERPING1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614457C>G , CM000673.2:g.57614457C>G	GRCh38
NC_000011.9:g.57381930C>G , CM000673.1:g.57381930C>G	GRCh37
NC_000011.8:g.57138506C>G	NCBI36
NG_009625.1:g.21904C>G , LRG_105:g.21904C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000062.3:c.1379C>G MANE Select	NP_000053.2:p.Ser460Cys
ENST00000278407.9:c.1379C>G MANE Select	ENSP00000278407.4:p.Ser460Cys
NM_000062.2:c.1379C>G , LRG_105t1:c.1379C>G	NP_000053.2:p.Ser460Cys
NM_001032295.1:c.1379C>G	NP_001027466.1:p.Ser460Cys
NM_001032295.2:c.1379C>G	NP_001027466.1:p.Ser460Cys
ENST00000278407.8:c.1379C>G	ENSP00000278407.4:p.Ser460Cys
ENST00000340687.10:c.1268C>G	ENSP00000341861.6:p.Ser423Cys
ENST00000378323.8:c.1394C>G	ENSP00000367574.4:p.Ser465Cys
ENST00000378324.6:c.1223C>G	ENSP00000367575.2:p.Ser408Cys
ENST00000403558.1:c.1508C>G	ENSP00000384420.1:p.Ser503Cys
ENST00000528996.1:c.580C>G	ENSP00000431226.1:n.580C>G
ENST00000528996.2:c.*276C>G	ENSP00000431226.2:n.*276C>G
ENST00000530113.1:n.836C>G
ENST00000531133.5:c.880C>G	ENSP00000435431.1:n.880C>G
ENST00000531605.2:c.*1155C>G	ENSP00000503752.1:n.*1155C>G
ENST00000531797.5:c.*404C>G	ENSP00000432554.1:n.*404C>G
ENST00000619430.1:c.510C>G	ENSP00000478572.1:n.510C>G
ENST00000619430.2:c.1175C>G	ENSP00000478572.2:p.Ser392Cys
ENST00000676670.1:c.1379C>G	ENSP00000504807.1:p.Ser460Cys
ENST00000676741.1:n.2461C>G
ENST00000677624.1:c.*799C>G	ENSP00000503979.1:n.*799C>G
ENST00000677625.1:c.1325C>G	ENSP00000502857.1:p.Ser442Cys
ENST00000677856.1:n.1632C>G
ENST00000677915.1:c.*276C>G	ENSP00000503118.1:n.*276C>G
ENST00000678533.1:c.*933C>G	ENSP00000503873.1:n.*933C>G
ENST00000678592.1:c.*319C>G	ENSP00000504424.1:n.*319C>G