Canonical Allele Identifier: CA380703493

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57379390C>A (hg19) ; chr11:g.57611917C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611917C>A , CM000673.2:g.57611917C>A	GRCh38
NC_000011.9:g.57379390C>A , CM000673.1:g.57379390C>A	GRCh37
NC_000011.8:g.57135966C>A	NCBI36
NG_009625.1:g.19364C>A , LRG_105:g.19364C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1230C>A MANE Select	ENSP00000278407.4:p.Leu410=
ENST00000528996.2:c.*127C>A	ENSP00000431226.2:n.*127C>A
ENST00000531605.2:c.*1006C>A	ENSP00000503752.1:n.*1006C>A
ENST00000619430.2:c.1026C>A	ENSP00000478572.2:p.Leu342=
ENST00000676670.1:c.1230C>A	ENSP00000504807.1:p.Leu410=
ENST00000676741.1:n.2312C>A
ENST00000677624.1:c.*650C>A	ENSP00000503979.1:n.*650C>A
ENST00000677625.1:c.1176C>A	ENSP00000502857.1:p.Leu392=
ENST00000677856.1:n.1483C>A
ENST00000677915.1:c.*127C>A	ENSP00000503118.1:n.*127C>A
ENST00000678533.1:c.*784C>A	ENSP00000503873.1:n.*784C>A
ENST00000678592.1:c.*170C>A	ENSP00000504424.1:n.*170C>A
ENST00000278407.8:c.1230C>A	ENSP00000278407.4:p.Leu410=
ENST00000340687.10:c.1119C>A	ENSP00000341861.6:p.Leu373=
ENST00000378323.8:c.1245C>A	ENSP00000367574.4:p.Leu415=
ENST00000378324.6:c.1074C>A	ENSP00000367575.2:p.Leu358=
ENST00000403558.1:c.1359C>A	ENSP00000384420.1:p.Leu453=
ENST00000528996.1:c.431C>A	ENSP00000431226.1:n.431C>A
ENST00000530113.1:n.687C>A
ENST00000531133.5:c.731C>A	ENSP00000435431.1:n.731C>A
ENST00000531797.5:c.*255C>A	ENSP00000432554.1:n.*255C>A
ENST00000619430.1:c.361C>A	ENSP00000478572.1:p.Leu121Ile
NM_000062.2:c.1230C>A , LRG_105t1:c.1230C>A	NP_000053.2:p.Leu410=
NM_001032295.1:c.1230C>A	NP_001027466.1:p.Leu410=
NM_000062.3:c.1230C>A MANE Select	NP_000053.2:p.Leu410=
NM_001032295.2:c.1230C>A	NP_001027466.1:p.Leu410=