Canonical Allele Identifier: CA474568254
Gene: SERPING1 HGNC NCBI

Linked Data

dbSNP Id: rs1945479878
MyVariant Identifiers: chr11:g.57379330G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57611857G>A , CM000673.2:g.57611857G>A GRCh38
NC_000011.9:g.57379330G>A , CM000673.1:g.57379330G>A GRCh37
NC_000011.8:g.57135906G>A NCBI36
NG_009625.1:g.19304G>A , LRG_105:g.19304G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000278407.9:c.1170G>A MANE Select ENSP00000278407.4:p.Lys390=
ENST00000528996.2:c.*67G>A ENSP00000431226.2:n.*67G>A
ENST00000531605.2:c.*946G>A ENSP00000503752.1:n.*946G>A
ENST00000619430.2:c.966G>A ENSP00000478572.2:p.Lys322=
ENST00000676670.1:c.1170G>A ENSP00000504807.1:p.Lys390=
ENST00000676741.1:n.2252G>A
ENST00000677624.1:c.*590G>A ENSP00000503979.1:n.*590G>A
ENST00000677625.1:c.1116G>A ENSP00000502857.1:p.Lys372=
ENST00000677856.1:n.1423G>A
ENST00000677915.1:c.*67G>A ENSP00000503118.1:n.*67G>A
ENST00000678533.1:c.*724G>A ENSP00000503873.1:n.*724G>A
ENST00000678592.1:c.*110G>A ENSP00000504424.1:n.*110G>A
ENST00000278407.8:c.1170G>A ENSP00000278407.4:p.Lys390=
ENST00000340687.10:c.1059G>A ENSP00000341861.6:p.Lys353=
ENST00000378323.8:c.1185G>A ENSP00000367574.4:p.Lys395=
ENST00000378324.6:c.1014G>A ENSP00000367575.2:p.Lys338=
ENST00000403558.1:c.1299G>A ENSP00000384420.1:p.Lys433=
ENST00000528996.1:c.371G>A ENSP00000431226.1:n.371G>A
ENST00000530113.1:n.627G>A
ENST00000531133.5:c.671G>A ENSP00000435431.1:n.671G>A
ENST00000531797.5:c.*195G>A ENSP00000432554.1:n.*195G>A
ENST00000619430.1:c.349-48G>A ENSP00000478572.1:n.349-48G>A
NM_000062.2:c.1170G>A , LRG_105t1:c.1170G>A NP_000053.2:p.Lys390=
NM_001032295.1:c.1170G>A NP_001027466.1:p.Lys390=
NM_000062.3:c.1170G>A MANE Select NP_000053.2:p.Lys390=
NM_001032295.2:c.1170G>A NP_001027466.1:p.Lys390=