Canonical Allele Identifier: CA380690108

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381801A>G (hg19) ; chr11:g.57614328A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614328A>G , CM000673.2:g.57614328A>G	GRCh38
NC_000011.9:g.57381801A>G , CM000673.1:g.57381801A>G	GRCh37
NC_000011.8:g.57138377A>G	NCBI36
NG_009625.1:g.21775A>G , LRG_105:g.21775A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1250A>G MANE Select	ENSP00000278407.4:p.Glu417Gly
ENST00000528996.2:c.*147A>G	ENSP00000431226.2:n.*147A>G
ENST00000531605.2:c.*1026A>G	ENSP00000503752.1:n.*1026A>G
ENST00000619430.2:c.1046A>G	ENSP00000478572.2:p.Glu349Gly
ENST00000676670.1:c.1250A>G	ENSP00000504807.1:p.Glu417Gly
ENST00000676741.1:n.2332A>G
ENST00000677624.1:c.*670A>G	ENSP00000503979.1:n.*670A>G
ENST00000677625.1:c.1196A>G	ENSP00000502857.1:p.Glu399Gly
ENST00000677856.1:n.1503A>G
ENST00000677915.1:c.*147A>G	ENSP00000503118.1:n.*147A>G
ENST00000678533.1:c.*804A>G	ENSP00000503873.1:n.*804A>G
ENST00000678592.1:c.*190A>G	ENSP00000504424.1:n.*190A>G
ENST00000278407.8:c.1250A>G	ENSP00000278407.4:p.Glu417Gly
ENST00000340687.10:c.1139A>G	ENSP00000341861.6:p.Glu380Gly
ENST00000378323.8:c.1265A>G	ENSP00000367574.4:p.Glu422Gly
ENST00000378324.6:c.1094A>G	ENSP00000367575.2:p.Glu365Gly
ENST00000403558.1:c.1379A>G	ENSP00000384420.1:p.Glu460Gly
ENST00000528996.1:c.451A>G	ENSP00000431226.1:n.451A>G
ENST00000530113.1:n.707A>G
ENST00000531133.5:c.751A>G	ENSP00000435431.1:n.751A>G
ENST00000531797.5:c.*275A>G	ENSP00000432554.1:n.*275A>G
ENST00000619430.1:c.381A>G	ENSP00000478572.1:p.Gly127=
NM_000062.2:c.1250A>G , LRG_105t1:c.1250A>G	NP_000053.2:p.Glu417Gly
NM_001032295.1:c.1250A>G	NP_001027466.1:p.Glu417Gly
NM_000062.3:c.1250A>G MANE Select	NP_000053.2:p.Glu417Gly
NM_001032295.2:c.1250A>G	NP_001027466.1:p.Glu417Gly