Canonical Allele Identifier: CA474566435
Gene: SERPING1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.57373502C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57606029C>T , CM000673.2:g.57606029C>T GRCh38
NC_000011.9:g.57373502C>T , CM000673.1:g.57373502C>T GRCh37
NC_000011.8:g.57130078C>T NCBI36
NG_009625.1:g.13476C>T , LRG_105:g.13476C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.705C>T MANE Select ENSP00000278407.4:p.Thr235=
ENST00000528996.2:c.59-5697C>T ENSP00000431226.2:n.59-5697C>T
ENST00000531605.2:c.*481C>T ENSP00000503752.1:n.*481C>T
ENST00000619430.2:c.686-379C>T ENSP00000478572.2:n.686-379C>T
ENST00000676670.1:c.705C>T ENSP00000504807.1:p.Thr235=
ENST00000676741.1:n.1787C>T
ENST00000677624.1:c.*125C>T ENSP00000503979.1:n.*125C>T
ENST00000677625.1:c.705C>T ENSP00000502857.1:p.Thr235=
ENST00000677856.1:n.764C>T
ENST00000677915.1:c.685+3860C>T ENSP00000503118.1:n.685+3860C>T
ENST00000678533.1:c.*259C>T ENSP00000503873.1:n.*259C>T
ENST00000678592.1:c.705C>T ENSP00000504424.1:p.Thr235=
ENST00000278407.8:c.705C>T ENSP00000278407.4:p.Thr235=
ENST00000340687.10:c.705C>T ENSP00000341861.6:p.Thr235=
ENST00000378323.8:c.720C>T ENSP00000367574.4:p.Thr240=
ENST00000378324.6:c.549C>T ENSP00000367575.2:p.Thr183=
ENST00000403558.1:c.807C>T ENSP00000384420.1:p.Thr269=
ENST00000531133.5:c.206C>T ENSP00000435431.1:n.206C>T
ENST00000531605.1:n.552C>T
ENST00000531797.5:c.*54+3860C>T ENSP00000432554.1:n.*54+3860C>T
ENST00000619430.1:c.348+5854C>T ENSP00000478572.1:n.348+5854C>T
NM_000062.2:c.705C>T , LRG_105t1:c.705C>T NP_000053.2:p.Thr235=
NM_001032295.1:c.705C>T NP_001027466.1:p.Thr235=
NM_000062.3:c.705C>T MANE Select NP_000053.2:p.Thr235=
NM_001032295.2:c.705C>T NP_001027466.1:p.Thr235=