Canonical Allele Identifier: CA380690838

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381993T>A (hg19) ; chr11:g.57614520T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614520T>A , CM000673.2:g.57614520T>A	GRCh38
NC_000011.9:g.57381993T>A , CM000673.1:g.57381993T>A	GRCh37
NC_000011.8:g.57138569T>A	NCBI36
NG_009625.1:g.21967T>A , LRG_105:g.21967T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1442T>A MANE Select	ENSP00000278407.4:p.Leu481His
ENST00000528996.2:c.*339T>A	ENSP00000431226.2:n.*339T>A
ENST00000531605.2:c.*1218T>A	ENSP00000503752.1:n.*1218T>A
ENST00000619430.2:c.1238T>A	ENSP00000478572.2:p.Leu413His
ENST00000676670.1:c.1442T>A	ENSP00000504807.1:p.Leu481His
ENST00000676741.1:n.2524T>A
ENST00000677624.1:c.*862T>A	ENSP00000503979.1:n.*862T>A
ENST00000677625.1:c.1388T>A	ENSP00000502857.1:p.Leu463His
ENST00000677856.1:n.1695T>A
ENST00000677915.1:c.*339T>A	ENSP00000503118.1:n.*339T>A
ENST00000678533.1:c.*996T>A	ENSP00000503873.1:n.*996T>A
ENST00000678592.1:c.*382T>A	ENSP00000504424.1:n.*382T>A
ENST00000278407.8:c.1442T>A	ENSP00000278407.4:p.Leu481His
ENST00000340687.10:c.1331T>A	ENSP00000341861.6:p.Leu444His
ENST00000378323.8:c.1457T>A	ENSP00000367574.4:p.Leu486His
ENST00000378324.6:c.1286T>A	ENSP00000367575.2:p.Leu429His
ENST00000403558.1:c.1571T>A	ENSP00000384420.1:p.Leu524His
ENST00000528996.1:c.643T>A	ENSP00000431226.1:n.643T>A
ENST00000530113.1:n.899T>A
ENST00000531133.5:c.943T>A	ENSP00000435431.1:n.943T>A
ENST00000531797.5:c.*467T>A	ENSP00000432554.1:n.*467T>A
ENST00000619430.1:c.573T>A	ENSP00000478572.1:n.573T>A
NM_000062.2:c.1442T>A , LRG_105t1:c.1442T>A	NP_000053.2:p.Leu481His
NM_001032295.1:c.1442T>A	NP_001027466.1:p.Leu481His
NM_000062.3:c.1442T>A MANE Select	NP_000053.2:p.Leu481His
NM_001032295.2:c.1442T>A	NP_001027466.1:p.Leu481His