Canonical Allele Identifier: CA380702294
Gene: SERPING1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57611724A>C , CM000673.2:g.57611724A>C GRCh38
NC_000011.9:g.57379197A>C , CM000673.1:g.57379197A>C GRCh37
NC_000011.8:g.57135773A>C NCBI36
NG_009625.1:g.19171A>C , LRG_105:g.19171A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.1037A>C MANE Select ENSP00000278407.4:p.Gln346Pro
ENST00000528996.2:c.59-2A>C ENSP00000431226.2:n.59-2A>C
ENST00000531605.2:c.*813A>C ENSP00000503752.1:n.*813A>C
ENST00000619430.2:c.833A>C ENSP00000478572.2:p.Gln278Pro
ENST00000676670.1:c.1037A>C ENSP00000504807.1:p.Gln346Pro
ENST00000676741.1:n.2119A>C
ENST00000677624.1:c.*457A>C ENSP00000503979.1:n.*457A>C
ENST00000677625.1:c.1030-47A>C ENSP00000502857.1:n.1030-47A>C
ENST00000677856.1:n.1290A>C
ENST00000677915.1:c.693A>C ENSP00000503118.1:p.Ala231=
ENST00000678533.1:c.*591A>C ENSP00000503873.1:n.*591A>C
ENST00000678592.1:c.1126A>C ENSP00000504424.1:p.Ser376Arg
ENST00000278407.8:c.1037A>C ENSP00000278407.4:p.Gln346Pro
ENST00000340687.10:c.1030-104A>C ENSP00000341861.6:n.1030-104A>C
ENST00000378323.8:c.1052A>C ENSP00000367574.4:p.Gln351Pro
ENST00000378324.6:c.881A>C ENSP00000367575.2:p.Gln294Pro
ENST00000403558.1:c.1166A>C ENSP00000384420.1:p.Gln389Pro
ENST00000528996.1:c.238A>C ENSP00000431226.1:p.Ser80Arg
ENST00000530113.1:n.494A>C
ENST00000531133.5:c.538A>C ENSP00000435431.1:n.538A>C
ENST00000531797.5:c.*62A>C ENSP00000432554.1:n.*62A>C
ENST00000619430.1:c.349-181A>C ENSP00000478572.1:n.349-181A>C
NM_000062.2:c.1037A>C , LRG_105t1:c.1037A>C NP_000053.2:p.Gln346Pro
NM_001032295.1:c.1037A>C NP_001027466.1:p.Gln346Pro
NM_000062.3:c.1037A>C MANE Select NP_000053.2:p.Gln346Pro
NM_001032295.2:c.1037A>C NP_001027466.1:p.Gln346Pro