Canonical Allele Identifier: CA380690831

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381990T>A (hg19) ; chr11:g.57614517T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614517T>A , CM000673.2:g.57614517T>A	GRCh38
NC_000011.9:g.57381990T>A , CM000673.1:g.57381990T>A	GRCh37
NC_000011.8:g.57138566T>A	NCBI36
NG_009625.1:g.21964T>A , LRG_105:g.21964T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1439T>A MANE Select	ENSP00000278407.4:p.Val480Glu
ENST00000528996.2:c.*336T>A	ENSP00000431226.2:n.*336T>A
ENST00000531605.2:c.*1215T>A	ENSP00000503752.1:n.*1215T>A
ENST00000619430.2:c.1235T>A	ENSP00000478572.2:p.Val412Glu
ENST00000676670.1:c.1439T>A	ENSP00000504807.1:p.Val480Glu
ENST00000676741.1:n.2521T>A
ENST00000677624.1:c.*859T>A	ENSP00000503979.1:n.*859T>A
ENST00000677625.1:c.1385T>A	ENSP00000502857.1:p.Val462Glu
ENST00000677856.1:n.1692T>A
ENST00000677915.1:c.*336T>A	ENSP00000503118.1:n.*336T>A
ENST00000678533.1:c.*993T>A	ENSP00000503873.1:n.*993T>A
ENST00000678592.1:c.*379T>A	ENSP00000504424.1:n.*379T>A
ENST00000278407.8:c.1439T>A	ENSP00000278407.4:p.Val480Glu
ENST00000340687.10:c.1328T>A	ENSP00000341861.6:p.Val443Glu
ENST00000378323.8:c.1454T>A	ENSP00000367574.4:p.Val485Glu
ENST00000378324.6:c.1283T>A	ENSP00000367575.2:p.Val428Glu
ENST00000403558.1:c.1568T>A	ENSP00000384420.1:p.Val523Glu
ENST00000528996.1:c.640T>A	ENSP00000431226.1:n.640T>A
ENST00000530113.1:n.896T>A
ENST00000531133.5:c.940T>A	ENSP00000435431.1:n.940T>A
ENST00000531797.5:c.*464T>A	ENSP00000432554.1:n.*464T>A
ENST00000619430.1:c.570T>A	ENSP00000478572.1:n.570T>A
NM_000062.2:c.1439T>A , LRG_105t1:c.1439T>A	NP_000053.2:p.Val480Glu
NM_001032295.1:c.1439T>A	NP_001027466.1:p.Val480Glu
NM_000062.3:c.1439T>A MANE Select	NP_000053.2:p.Val480Glu
NM_001032295.2:c.1439T>A	NP_001027466.1:p.Val480Glu