Canonical Allele Identifier: CA380702678

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57379256C>G (hg19) ; chr11:g.57611783C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611783C>G , CM000673.2:g.57611783C>G	GRCh38
NC_000011.9:g.57379256C>G , CM000673.1:g.57379256C>G	GRCh37
NC_000011.8:g.57135832C>G	NCBI36
NG_009625.1:g.19230C>G , LRG_105:g.19230C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1096C>G MANE Select	ENSP00000278407.4:p.Arg366Gly
ENST00000528996.2:c.116C>G	ENSP00000431226.2:p.Ser39Trp
ENST00000531605.2:c.*872C>G	ENSP00000503752.1:n.*872C>G
ENST00000619430.2:c.892C>G	ENSP00000478572.2:p.Arg298Gly
ENST00000676670.1:c.1096C>G	ENSP00000504807.1:p.Arg366Gly
ENST00000676741.1:n.2178C>G
ENST00000677624.1:c.*516C>G	ENSP00000503979.1:n.*516C>G
ENST00000677625.1:c.1042C>G	ENSP00000502857.1:p.Arg348Gly
ENST00000677856.1:n.1349C>G
ENST00000677915.1:c.752C>G	ENSP00000503118.1:p.Ser251Trp
ENST00000678533.1:c.*650C>G	ENSP00000503873.1:n.*650C>G
ENST00000678592.1:c.*36C>G	ENSP00000504424.1:n.*36C>G
ENST00000278407.8:c.1096C>G	ENSP00000278407.4:p.Arg366Gly
ENST00000340687.10:c.1030-45C>G	ENSP00000341861.6:n.1030-45C>G
ENST00000378323.8:c.1111C>G	ENSP00000367574.4:p.Arg371Gly
ENST00000378324.6:c.940C>G	ENSP00000367575.2:p.Arg314Gly
ENST00000403558.1:c.1225C>G	ENSP00000384420.1:p.Arg409Gly
ENST00000528996.1:c.297C>G	ENSP00000431226.1:n.297C>G
ENST00000530113.1:n.553C>G
ENST00000531133.5:c.597C>G	ENSP00000435431.1:n.597C>G
ENST00000531797.5:c.*121C>G	ENSP00000432554.1:n.*121C>G
ENST00000619430.1:c.349-122C>G	ENSP00000478572.1:n.349-122C>G
NM_000062.2:c.1096C>G , LRG_105t1:c.1096C>G	NP_000053.2:p.Arg366Gly
NM_001032295.1:c.1096C>G	NP_001027466.1:p.Arg366Gly
NM_000062.3:c.1096C>G MANE Select	NP_000053.2:p.Arg366Gly
NM_001032295.2:c.1096C>G	NP_001027466.1:p.Arg366Gly