Canonical Allele Identifier: CA474807098
Gene: SERPING1 HGNC NCBI

Linked Data

dbSNP Id: rs2135308505
MyVariant Identifiers: chr11:g.57367618T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57600145T>A , CM000673.2:g.57600145T>A GRCh38
NC_000011.9:g.57367618T>A , CM000673.1:g.57367618T>A GRCh37
NC_000011.8:g.57124194T>A NCBI36
NG_009625.1:g.7592T>A , LRG_105:g.7592T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.318T>A MANE Select ENSP00000278407.4:p.Thr106=
ENST00000528996.2:c.58+1817T>A ENSP00000431226.2:n.58+1817T>A
ENST00000531605.2:c.51+1824T>A ENSP00000503752.1:n.51+1824T>A
ENST00000619430.2:c.318T>A ENSP00000478572.2:p.Thr106=
ENST00000676670.1:c.318T>A ENSP00000504807.1:p.Thr106=
ENST00000676741.1:n.1400T>A
ENST00000677275.1:n.305T>A
ENST00000677624.1:c.318T>A ENSP00000503979.1:p.Thr106=
ENST00000677625.1:c.318T>A ENSP00000502857.1:p.Thr106=
ENST00000677856.1:n.377T>A
ENST00000677915.1:c.318T>A ENSP00000503118.1:p.Thr106=
ENST00000678533.1:c.51+1824T>A ENSP00000503873.1:n.51+1824T>A
ENST00000678592.1:c.318T>A ENSP00000504424.1:p.Thr106=
ENST00000278407.8:c.318T>A ENSP00000278407.4:p.Thr106=
ENST00000340687.10:c.318T>A ENSP00000341861.6:p.Thr106=
ENST00000378323.8:c.333T>A ENSP00000367574.4:p.Thr111=
ENST00000378324.6:c.162T>A ENSP00000367575.2:p.Thr54=
ENST00000403558.1:c.420T>A ENSP00000384420.1:p.Thr140=
ENST00000405496.5:c.318T>A ENSP00000384561.1:p.Thr106=
ENST00000531133.5:c.51+1824T>A ENSP00000435431.1:n.51+1824T>A
ENST00000531797.5:c.51+1824T>A ENSP00000432554.1:n.51+1824T>A
ENST00000619430.1:c.318T>A ENSP00000478572.1:p.Thr106=
NM_000062.2:c.318T>A , LRG_105t1:c.318T>A NP_000053.2:p.Thr106=
NM_001032295.1:c.318T>A NP_001027466.1:p.Thr106=
NM_000062.3:c.318T>A MANE Select NP_000053.2:p.Thr106=
NM_001032295.2:c.318T>A NP_001027466.1:p.Thr106=