Canonical Allele Identifier: CA380690695

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381921C>T (hg19) ; chr11:g.57614448C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614448C>T , CM000673.2:g.57614448C>T	GRCh38
NC_000011.9:g.57381921C>T , CM000673.1:g.57381921C>T	GRCh37
NC_000011.8:g.57138497C>T	NCBI36
NG_009625.1:g.21895C>T , LRG_105:g.21895C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1370C>T MANE Select	ENSP00000278407.4:p.Ala457Val
ENST00000528996.2:c.*267C>T	ENSP00000431226.2:n.*267C>T
ENST00000531605.2:c.*1146C>T	ENSP00000503752.1:n.*1146C>T
ENST00000619430.2:c.1166C>T	ENSP00000478572.2:p.Ala389Val
ENST00000676670.1:c.1370C>T	ENSP00000504807.1:p.Ala457Val
ENST00000676741.1:n.2452C>T
ENST00000677624.1:c.*790C>T	ENSP00000503979.1:n.*790C>T
ENST00000677625.1:c.1316C>T	ENSP00000502857.1:p.Ala439Val
ENST00000677856.1:n.1623C>T
ENST00000677915.1:c.*267C>T	ENSP00000503118.1:n.*267C>T
ENST00000678533.1:c.*924C>T	ENSP00000503873.1:n.*924C>T
ENST00000678592.1:c.*310C>T	ENSP00000504424.1:n.*310C>T
ENST00000278407.8:c.1370C>T	ENSP00000278407.4:p.Ala457Val
ENST00000340687.10:c.1259C>T	ENSP00000341861.6:p.Ala420Val
ENST00000378323.8:c.1385C>T	ENSP00000367574.4:p.Ala462Val
ENST00000378324.6:c.1214C>T	ENSP00000367575.2:p.Ala405Val
ENST00000403558.1:c.1499C>T	ENSP00000384420.1:p.Ala500Val
ENST00000528996.1:c.571C>T	ENSP00000431226.1:n.571C>T
ENST00000530113.1:n.827C>T
ENST00000531133.5:c.871C>T	ENSP00000435431.1:n.871C>T
ENST00000531797.5:c.*395C>T	ENSP00000432554.1:n.*395C>T
ENST00000619430.1:c.501C>T	ENSP00000478572.1:n.501C>T
NM_000062.2:c.1370C>T , LRG_105t1:c.1370C>T	NP_000053.2:p.Ala457Val
NM_001032295.1:c.1370C>T	NP_001027466.1:p.Ala457Val
NM_000062.3:c.1370C>T MANE Select	NP_000053.2:p.Ala457Val
NM_001032295.2:c.1370C>T	NP_001027466.1:p.Ala457Val