Canonical Allele Identifier: CA380690879

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57382009C>G (hg19) ; chr11:g.57614536C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614536C>G , CM000673.2:g.57614536C>G	GRCh38
NC_000011.9:g.57382009C>G , CM000673.1:g.57382009C>G	GRCh37
NC_000011.8:g.57138585C>G	NCBI36
NG_009625.1:g.21983C>G , LRG_105:g.21983C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1458C>G MANE Select	ENSP00000278407.4:p.His486Gln
ENST00000528996.2:c.*355C>G	ENSP00000431226.2:n.*355C>G
ENST00000531605.2:c.*1234C>G	ENSP00000503752.1:n.*1234C>G
ENST00000619430.2:c.1254C>G	ENSP00000478572.2:p.His418Gln
ENST00000676670.1:c.1458C>G	ENSP00000504807.1:p.His486Gln
ENST00000676741.1:n.2540C>G
ENST00000677624.1:c.*878C>G	ENSP00000503979.1:n.*878C>G
ENST00000677625.1:c.1404C>G	ENSP00000502857.1:p.His468Gln
ENST00000677856.1:n.1711C>G
ENST00000677915.1:c.*355C>G	ENSP00000503118.1:n.*355C>G
ENST00000678533.1:c.*1012C>G	ENSP00000503873.1:n.*1012C>G
ENST00000678592.1:c.*398C>G	ENSP00000504424.1:n.*398C>G
ENST00000278407.8:c.1458C>G	ENSP00000278407.4:p.His486Gln
ENST00000340687.10:c.1347C>G	ENSP00000341861.6:p.His449Gln
ENST00000378323.8:c.1473C>G	ENSP00000367574.4:p.His491Gln
ENST00000378324.6:c.1302C>G	ENSP00000367575.2:p.His434Gln
ENST00000403558.1:c.1587C>G	ENSP00000384420.1:p.His529Gln
ENST00000528996.1:c.659C>G	ENSP00000431226.1:n.659C>G
ENST00000531133.5:c.959C>G	ENSP00000435431.1:n.959C>G
ENST00000531797.5:c.*483C>G	ENSP00000432554.1:n.*483C>G
ENST00000619430.1:c.589C>G	ENSP00000478572.1:n.589C>G
NM_000062.2:c.1458C>G , LRG_105t1:c.1458C>G	NP_000053.2:p.His486Gln
NM_001032295.1:c.1458C>G	NP_001027466.1:p.His486Gln
NM_000062.3:c.1458C>G MANE Select	NP_000053.2:p.His486Gln
NM_001032295.2:c.1458C>G	NP_001027466.1:p.His486Gln