Canonical Allele Identifier: CA380690751

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381954T>A (hg19) ; chr11:g.57614481T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614481T>A , CM000673.2:g.57614481T>A	GRCh38
NC_000011.9:g.57381954T>A , CM000673.1:g.57381954T>A	GRCh37
NC_000011.8:g.57138530T>A	NCBI36
NG_009625.1:g.21928T>A , LRG_105:g.21928T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1403T>A MANE Select	ENSP00000278407.4:p.Leu468Gln
ENST00000528996.2:c.*300T>A	ENSP00000431226.2:n.*300T>A
ENST00000531605.2:c.*1179T>A	ENSP00000503752.1:n.*1179T>A
ENST00000619430.2:c.1199T>A	ENSP00000478572.2:p.Leu400Gln
ENST00000676670.1:c.1403T>A	ENSP00000504807.1:p.Leu468Gln
ENST00000676741.1:n.2485T>A
ENST00000677624.1:c.*823T>A	ENSP00000503979.1:n.*823T>A
ENST00000677625.1:c.1349T>A	ENSP00000502857.1:p.Leu450Gln
ENST00000677856.1:n.1656T>A
ENST00000677915.1:c.*300T>A	ENSP00000503118.1:n.*300T>A
ENST00000678533.1:c.*957T>A	ENSP00000503873.1:n.*957T>A
ENST00000678592.1:c.*343T>A	ENSP00000504424.1:n.*343T>A
ENST00000278407.8:c.1403T>A	ENSP00000278407.4:p.Leu468Gln
ENST00000340687.10:c.1292T>A	ENSP00000341861.6:p.Leu431Gln
ENST00000378323.8:c.1418T>A	ENSP00000367574.4:p.Leu473Gln
ENST00000378324.6:c.1247T>A	ENSP00000367575.2:p.Leu416Gln
ENST00000403558.1:c.1532T>A	ENSP00000384420.1:p.Leu511Gln
ENST00000528996.1:c.604T>A	ENSP00000431226.1:n.604T>A
ENST00000530113.1:n.860T>A
ENST00000531133.5:c.904T>A	ENSP00000435431.1:n.904T>A
ENST00000531797.5:c.*428T>A	ENSP00000432554.1:n.*428T>A
ENST00000619430.1:c.534T>A	ENSP00000478572.1:n.534T>A
NM_000062.2:c.1403T>A , LRG_105t1:c.1403T>A	NP_000053.2:p.Leu468Gln
NM_001032295.1:c.1403T>A	NP_001027466.1:p.Leu468Gln
NM_000062.3:c.1403T>A MANE Select	NP_000053.2:p.Leu468Gln
NM_001032295.2:c.1403T>A	NP_001027466.1:p.Leu468Gln