Canonical Allele Identifier: CA380690319

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381839C>G (hg19) ; chr11:g.57614366C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614366C>G , CM000673.2:g.57614366C>G	GRCh38
NC_000011.9:g.57381839C>G , CM000673.1:g.57381839C>G	GRCh37
NC_000011.8:g.57138415C>G	NCBI36
NG_009625.1:g.21813C>G , LRG_105:g.21813C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.1288C>G MANE Select	ENSP00000278407.4:p.Leu430Val
ENST00000528996.2:c.*185C>G	ENSP00000431226.2:n.*185C>G
ENST00000531605.2:c.*1064C>G	ENSP00000503752.1:n.*1064C>G
ENST00000619430.2:c.1084C>G	ENSP00000478572.2:p.Leu362Val
ENST00000676670.1:c.1288C>G	ENSP00000504807.1:p.Leu430Val
ENST00000676741.1:n.2370C>G
ENST00000677624.1:c.*708C>G	ENSP00000503979.1:n.*708C>G
ENST00000677625.1:c.1234C>G	ENSP00000502857.1:p.Leu412Val
ENST00000677856.1:n.1541C>G
ENST00000677915.1:c.*185C>G	ENSP00000503118.1:n.*185C>G
ENST00000678533.1:c.*842C>G	ENSP00000503873.1:n.*842C>G
ENST00000678592.1:c.*228C>G	ENSP00000504424.1:n.*228C>G
ENST00000278407.8:c.1288C>G	ENSP00000278407.4:p.Leu430Val
ENST00000340687.10:c.1177C>G	ENSP00000341861.6:p.Leu393Val
ENST00000378323.8:c.1303C>G	ENSP00000367574.4:p.Leu435Val
ENST00000378324.6:c.1132C>G	ENSP00000367575.2:p.Leu378Val
ENST00000403558.1:c.1417C>G	ENSP00000384420.1:p.Leu473Val
ENST00000528996.1:c.489C>G	ENSP00000431226.1:n.489C>G
ENST00000530113.1:n.745C>G
ENST00000531133.5:c.789C>G	ENSP00000435431.1:n.789C>G
ENST00000531797.5:c.*313C>G	ENSP00000432554.1:n.*313C>G
ENST00000619430.1:c.419C>G	ENSP00000478572.1:n.419C>G
NM_000062.2:c.1288C>G , LRG_105t1:c.1288C>G	NP_000053.2:p.Leu430Val
NM_001032295.1:c.1288C>G	NP_001027466.1:p.Leu430Val
NM_000062.3:c.1288C>G MANE Select	NP_000053.2:p.Leu430Val
NM_001032295.2:c.1288C>G	NP_001027466.1:p.Leu430Val