Canonical Allele Identifier: CA1975537139
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57611858T= , CM000673.2:g.57611858T= GRCh38
NC_000011.9:g.57379331T= , CM000673.1:g.57379331T= GRCh37
NC_000011.8:g.57135907T= NCBI36
NG_009625.1:g.19305T= , LRG_105:g.19305T=

Transcript Alleles

HGVS Amino-acid change
ENST00000278407.9:c.1171T= MANE Select ENSP00000278407.4:p.Phe391=
ENST00000528996.2:c.*68T= ENSP00000431226.2:n.*68T=
ENST00000531605.2:c.*947T= ENSP00000503752.1:n.*947T=
ENST00000619430.2:c.967T= ENSP00000478572.2:p.Phe323=
ENST00000676670.1:c.1171T= ENSP00000504807.1:p.Phe391=
ENST00000676741.1:n.2253T=
ENST00000677624.1:c.*591T= ENSP00000503979.1:n.*591T=
ENST00000677625.1:c.1117T= ENSP00000502857.1:p.Phe373=
ENST00000677856.1:n.1424T=
ENST00000677915.1:c.*68T= ENSP00000503118.1:n.*68T=
ENST00000678533.1:c.*725T= ENSP00000503873.1:n.*725T=
ENST00000678592.1:c.*111T= ENSP00000504424.1:n.*111T=
ENST00000278407.8:c.1171T= ENSP00000278407.4:p.Phe391=
ENST00000340687.10:c.1060T= ENSP00000341861.6:p.Phe354=
ENST00000378323.8:c.1186T= ENSP00000367574.4:p.Phe396=
ENST00000378324.6:c.1015T= ENSP00000367575.2:p.Phe339=
ENST00000403558.1:c.1300T= ENSP00000384420.1:p.Phe434=
ENST00000528996.1:c.372T= ENSP00000431226.1:n.372T=
ENST00000530113.1:n.628T=
ENST00000531133.5:c.672T= ENSP00000435431.1:n.672T=
ENST00000531797.5:c.*196T= ENSP00000432554.1:n.*196T=
ENST00000619430.1:c.349-47T= ENSP00000478572.1:n.349-47T=
NM_000062.2:c.1171T= , LRG_105t1:c.1171T= NP_000053.2:p.Phe391=
NM_001032295.1:c.1171T= NP_001027466.1:p.Phe391=
NM_000062.3:c.1171T= MANE Select NP_000053.2:p.Phe391=
NM_001032295.2:c.1171T= NP_001027466.1:p.Phe391=