Canonical Allele Identifier: CA474568296

Gene: SERPING1

Linked Data

• dbSNP Id: rs1590829755
• MyVariant Identifiers: chr11:g.57379336G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611863G>A , CM000673.2:g.57611863G>A	GRCh38
NC_000011.9:g.57379336G>A , CM000673.1:g.57379336G>A	GRCh37
NC_000011.8:g.57135912G>A	NCBI36
NG_009625.1:g.19310G>A , LRG_105:g.19310G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.1176G>A MANE Select	ENSP00000278407.4:p.Gln392=
ENST00000528996.2:c.*73G>A	ENSP00000431226.2:n.*73G>A
ENST00000531605.2:c.*952G>A	ENSP00000503752.1:n.*952G>A
ENST00000619430.2:c.972G>A	ENSP00000478572.2:p.Gln324=
ENST00000676670.1:c.1176G>A	ENSP00000504807.1:p.Gln392=
ENST00000676741.1:n.2258G>A
ENST00000677624.1:c.*596G>A	ENSP00000503979.1:n.*596G>A
ENST00000677625.1:c.1122G>A	ENSP00000502857.1:p.Gln374=
ENST00000677856.1:n.1429G>A
ENST00000677915.1:c.*73G>A	ENSP00000503118.1:n.*73G>A
ENST00000678533.1:c.*730G>A	ENSP00000503873.1:n.*730G>A
ENST00000678592.1:c.*116G>A	ENSP00000504424.1:n.*116G>A
ENST00000278407.8:c.1176G>A	ENSP00000278407.4:p.Gln392=
ENST00000340687.10:c.1065G>A	ENSP00000341861.6:p.Gln355=
ENST00000378323.8:c.1191G>A	ENSP00000367574.4:p.Gln397=
ENST00000378324.6:c.1020G>A	ENSP00000367575.2:p.Gln340=
ENST00000403558.1:c.1305G>A	ENSP00000384420.1:p.Gln435=
ENST00000528996.1:c.377G>A	ENSP00000431226.1:n.377G>A
ENST00000530113.1:n.633G>A
ENST00000531133.5:c.677G>A	ENSP00000435431.1:n.677G>A
ENST00000531797.5:c.*201G>A	ENSP00000432554.1:n.*201G>A
ENST00000619430.1:c.349-42G>A	ENSP00000478572.1:n.349-42G>A
NM_000062.2:c.1176G>A , LRG_105t1:c.1176G>A	NP_000053.2:p.Gln392=
NM_001032295.1:c.1176G>A	NP_001027466.1:p.Gln392=
NM_000062.3:c.1176G>A MANE Select	NP_000053.2:p.Gln392=
NM_001032295.2:c.1176G>A	NP_001027466.1:p.Gln392=