Canonical Allele Identifier: CA380703323

Gene: SERPING1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611879C>G , CM000673.2:g.57611879C>G	GRCh38
NC_000011.9:g.57379352C>G , CM000673.1:g.57379352C>G	GRCh37
NC_000011.8:g.57135928C>G	NCBI36
NG_009625.1:g.19326C>G , LRG_105:g.19326C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000062.3:c.1192C>G MANE Select	NP_000053.2:p.Leu398Val
ENST00000278407.9:c.1192C>G MANE Select	ENSP00000278407.4:p.Leu398Val
NM_000062.2:c.1192C>G , LRG_105t1:c.1192C>G	NP_000053.2:p.Leu398Val
NM_001032295.1:c.1192C>G	NP_001027466.1:p.Leu398Val
NM_001032295.2:c.1192C>G	NP_001027466.1:p.Leu398Val
ENST00000278407.8:c.1192C>G	ENSP00000278407.4:p.Leu398Val
ENST00000340687.10:c.1081C>G	ENSP00000341861.6:p.Leu361Val
ENST00000378323.8:c.1207C>G	ENSP00000367574.4:p.Leu403Val
ENST00000378324.6:c.1036C>G	ENSP00000367575.2:p.Leu346Val
ENST00000403558.1:c.1321C>G	ENSP00000384420.1:p.Leu441Val
ENST00000528996.1:c.393C>G	ENSP00000431226.1:n.393C>G
ENST00000528996.2:c.*89C>G	ENSP00000431226.2:n.*89C>G
ENST00000530113.1:n.649C>G
ENST00000531133.5:c.693C>G	ENSP00000435431.1:n.693C>G
ENST00000531605.2:c.*968C>G	ENSP00000503752.1:n.*968C>G
ENST00000531797.5:c.*217C>G	ENSP00000432554.1:n.*217C>G
ENST00000619430.1:c.349-26C>G	ENSP00000478572.1:n.349-26C>G
ENST00000619430.2:c.988C>G	ENSP00000478572.2:p.Leu330Val
ENST00000676670.1:c.1192C>G	ENSP00000504807.1:p.Leu398Val
ENST00000676741.1:n.2274C>G
ENST00000677624.1:c.*612C>G	ENSP00000503979.1:n.*612C>G
ENST00000677625.1:c.1138C>G	ENSP00000502857.1:p.Leu380Val
ENST00000677856.1:n.1445C>G
ENST00000677915.1:c.*89C>G	ENSP00000503118.1:n.*89C>G
ENST00000678533.1:c.*746C>G	ENSP00000503873.1:n.*746C>G
ENST00000678592.1:c.*132C>G	ENSP00000504424.1:n.*132C>G