Canonical Allele Identifier: CA380703354

Gene: SERPING1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611885C>A , CM000673.2:g.57611885C>A	GRCh38
NC_000011.9:g.57379358C>A , CM000673.1:g.57379358C>A	GRCh37
NC_000011.8:g.57135934C>A	NCBI36
NG_009625.1:g.19332C>A , LRG_105:g.19332C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1198C>A MANE Select	ENSP00000278407.4:p.Arg400Ser
ENST00000528996.2:c.*95C>A	ENSP00000431226.2:n.*95C>A
ENST00000531605.2:c.*974C>A	ENSP00000503752.1:n.*974C>A
ENST00000619430.2:c.994C>A	ENSP00000478572.2:p.Arg332Ser
ENST00000676670.1:c.1198C>A	ENSP00000504807.1:p.Arg400Ser
ENST00000676741.1:n.2280C>A
ENST00000677624.1:c.*618C>A	ENSP00000503979.1:n.*618C>A
ENST00000677625.1:c.1144C>A	ENSP00000502857.1:p.Arg382Ser
ENST00000677856.1:n.1451C>A
ENST00000677915.1:c.*95C>A	ENSP00000503118.1:n.*95C>A
ENST00000678533.1:c.*752C>A	ENSP00000503873.1:n.*752C>A
ENST00000678592.1:c.*138C>A	ENSP00000504424.1:n.*138C>A
ENST00000278407.8:c.1198C>A	ENSP00000278407.4:p.Arg400Ser
ENST00000340687.10:c.1087C>A	ENSP00000341861.6:p.Arg363Ser
ENST00000378323.8:c.1213C>A	ENSP00000367574.4:p.Arg405Ser
ENST00000378324.6:c.1042C>A	ENSP00000367575.2:p.Arg348Ser
ENST00000403558.1:c.1327C>A	ENSP00000384420.1:p.Arg443Ser
ENST00000528996.1:c.399C>A	ENSP00000431226.1:n.399C>A
ENST00000530113.1:n.655C>A
ENST00000531133.5:c.699C>A	ENSP00000435431.1:n.699C>A
ENST00000531797.5:c.*223C>A	ENSP00000432554.1:n.*223C>A
ENST00000619430.1:c.349-20C>A	ENSP00000478572.1:n.349-20C>A
NM_000062.2:c.1198C>A , LRG_105t1:c.1198C>A	NP_000053.2:p.Arg400Ser
NM_001032295.1:c.1198C>A	NP_001027466.1:p.Arg400Ser
NM_000062.3:c.1198C>A MANE Select	NP_000053.2:p.Arg400Ser
NM_001032295.2:c.1198C>A	NP_001027466.1:p.Arg400Ser