Canonical Allele Identifier: CA1975523583
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57600134A= , CM000673.2:g.57600134A= GRCh38
NC_000011.9:g.57367607A= , CM000673.1:g.57367607A= GRCh37
NC_000011.8:g.57124183A= NCBI36
NG_009625.1:g.7581A= , LRG_105:g.7581A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.307A= MANE Select ENSP00000278407.4:p.Thr103=
ENST00000528996.2:c.58+1806A= ENSP00000431226.2:n.58+1806A=
ENST00000531605.2:c.51+1813A= ENSP00000503752.1:n.51+1813A=
ENST00000619430.2:c.307A= ENSP00000478572.2:p.Thr103=
ENST00000676670.1:c.307A= ENSP00000504807.1:p.Thr103=
ENST00000676741.1:n.1389A=
ENST00000677275.1:n.294A=
ENST00000677624.1:c.307A= ENSP00000503979.1:p.Thr103=
ENST00000677625.1:c.307A= ENSP00000502857.1:p.Thr103=
ENST00000677856.1:n.366A=
ENST00000677915.1:c.307A= ENSP00000503118.1:p.Thr103=
ENST00000678533.1:c.51+1813A= ENSP00000503873.1:n.51+1813A=
ENST00000678592.1:c.307A= ENSP00000504424.1:p.Thr103=
ENST00000278407.8:c.307A= ENSP00000278407.4:p.Thr103=
ENST00000340687.10:c.307A= ENSP00000341861.6:p.Thr103=
ENST00000378323.8:c.322A= ENSP00000367574.4:p.Thr108=
ENST00000378324.6:c.151A= ENSP00000367575.2:p.Thr51=
ENST00000403558.1:c.409A= ENSP00000384420.1:p.Thr137=
ENST00000405496.5:c.307A= ENSP00000384561.1:p.Thr103=
ENST00000531133.5:c.51+1813A= ENSP00000435431.1:n.51+1813A=
ENST00000531797.5:c.51+1813A= ENSP00000432554.1:n.51+1813A=
ENST00000619430.1:c.307A= ENSP00000478572.1:p.Thr103=
NM_000062.2:c.307A= , LRG_105t1:c.307A= NP_000053.2:p.Thr103=
NM_001032295.1:c.307A= NP_001027466.1:p.Thr103=
NM_000062.3:c.307A= MANE Select NP_000053.2:p.Thr103=
NM_001032295.2:c.307A= NP_001027466.1:p.Thr103=