Canonical Allele Identifier: CA1975539290
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57614502A= , CM000673.2:g.57614502A= GRCh38
NC_000011.9:g.57381975A= , CM000673.1:g.57381975A= GRCh37
NC_000011.8:g.57138551A= NCBI36
NG_009625.1:g.21949A= , LRG_105:g.21949A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.1424A= MANE Select ENSP00000278407.4:p.Gln475=
ENST00000528996.2:c.*321A= ENSP00000431226.2:n.*321A=
ENST00000531605.2:c.*1200A= ENSP00000503752.1:n.*1200A=
ENST00000619430.2:c.1220A= ENSP00000478572.2:p.Gln407=
ENST00000676670.1:c.1424A= ENSP00000504807.1:p.Gln475=
ENST00000676741.1:n.2506A=
ENST00000677624.1:c.*844A= ENSP00000503979.1:n.*844A=
ENST00000677625.1:c.1370A= ENSP00000502857.1:p.Gln457=
ENST00000677856.1:n.1677A=
ENST00000677915.1:c.*321A= ENSP00000503118.1:n.*321A=
ENST00000678533.1:c.*978A= ENSP00000503873.1:n.*978A=
ENST00000678592.1:c.*364A= ENSP00000504424.1:n.*364A=
ENST00000278407.8:c.1424A= ENSP00000278407.4:p.Gln475=
ENST00000340687.10:c.1313A= ENSP00000341861.6:p.Gln438=
ENST00000378323.8:c.1439A= ENSP00000367574.4:p.Gln480=
ENST00000378324.6:c.1268A= ENSP00000367575.2:p.Gln423=
ENST00000403558.1:c.1553A= ENSP00000384420.1:p.Gln518=
ENST00000528996.1:c.625A= ENSP00000431226.1:n.625A=
ENST00000530113.1:n.881A=
ENST00000531133.5:c.925A= ENSP00000435431.1:n.925A=
ENST00000531797.5:c.*449A= ENSP00000432554.1:n.*449A=
ENST00000619430.1:c.555A= ENSP00000478572.1:n.555A=
NM_000062.2:c.1424A= , LRG_105t1:c.1424A= NP_000053.2:p.Gln475=
NM_001032295.1:c.1424A= NP_001027466.1:p.Gln475=
NM_000062.3:c.1424A= MANE Select NP_000053.2:p.Gln475=
NM_001032295.2:c.1424A= NP_001027466.1:p.Gln475=