Canonical Allele Identifier: CA380699778
Gene: SERPING1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57606203C>G , CM000673.2:g.57606203C>G GRCh38
NC_000011.9:g.57373676C>G , CM000673.1:g.57373676C>G GRCh37
NC_000011.8:g.57130252C>G NCBI36
NG_009625.1:g.13650C>G , LRG_105:g.13650C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.879C>G MANE Select ENSP00000278407.4:p.Ile293Met
ENST00000528996.2:c.59-5523C>G ENSP00000431226.2:n.59-5523C>G
ENST00000531605.2:c.*655C>G ENSP00000503752.1:n.*655C>G
ENST00000619430.2:c.686-205C>G ENSP00000478572.2:n.686-205C>G
ENST00000676670.1:c.879C>G ENSP00000504807.1:p.Ile293Met
ENST00000676741.1:n.1961C>G
ENST00000677624.1:c.*299C>G ENSP00000503979.1:n.*299C>G
ENST00000677625.1:c.879C>G ENSP00000502857.1:p.Ile293Met
ENST00000677856.1:n.938C>G
ENST00000677915.1:c.685+4034C>G ENSP00000503118.1:n.685+4034C>G
ENST00000678533.1:c.*433C>G ENSP00000503873.1:n.*433C>G
ENST00000678592.1:c.879C>G ENSP00000504424.1:p.Ile293Met
ENST00000278407.8:c.879C>G ENSP00000278407.4:p.Ile293Met
ENST00000340687.10:c.879C>G ENSP00000341861.6:p.Ile293Met
ENST00000378323.8:c.894C>G ENSP00000367574.4:p.Ile298Met
ENST00000378324.6:c.723C>G ENSP00000367575.2:p.Ile241Met
ENST00000403558.1:c.981C>G ENSP00000384420.1:p.Ile327Met
ENST00000531133.5:c.380C>G ENSP00000435431.1:n.380C>G
ENST00000531797.5:c.*54+4034C>G ENSP00000432554.1:n.*54+4034C>G
ENST00000619430.1:c.349-5702C>G ENSP00000478572.1:n.349-5702C>G
NM_000062.2:c.879C>G , LRG_105t1:c.879C>G NP_000053.2:p.Ile293Met
NM_001032295.1:c.879C>G NP_001027466.1:p.Ile293Met
NM_000062.3:c.879C>G MANE Select NP_000053.2:p.Ile293Met
NM_001032295.2:c.879C>G NP_001027466.1:p.Ile293Met