Canonical Allele Identifier: CA1975536895
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57611765C= , CM000673.2:g.57611765C= GRCh38
NC_000011.9:g.57379238C= , CM000673.1:g.57379238C= GRCh37
NC_000011.8:g.57135814C= NCBI36
NG_009625.1:g.19212C= , LRG_105:g.19212C=

Transcript Alleles

HGVS Amino-acid change
ENST00000278407.9:c.1078C= MANE Select ENSP00000278407.4:p.Pro360=
ENST00000528996.2:c.98C= ENSP00000431226.2:p.Thr33=
ENST00000531605.2:c.*854C= ENSP00000503752.1:n.*854C=
ENST00000619430.2:c.874C= ENSP00000478572.2:p.Pro292=
ENST00000676670.1:c.1078C= ENSP00000504807.1:p.Pro360=
ENST00000676741.1:n.2160C=
ENST00000677624.1:c.*498C= ENSP00000503979.1:n.*498C=
ENST00000677625.1:c.1030-6C= ENSP00000502857.1:n.1030-6C=
ENST00000677856.1:n.1331C=
ENST00000677915.1:c.734C= ENSP00000503118.1:p.Thr245=
ENST00000678533.1:c.*632C= ENSP00000503873.1:n.*632C=
ENST00000678592.1:c.*18C= ENSP00000504424.1:n.*18C=
ENST00000278407.8:c.1078C= ENSP00000278407.4:p.Pro360=
ENST00000340687.10:c.1030-63C= ENSP00000341861.6:n.1030-63C=
ENST00000378323.8:c.1093C= ENSP00000367574.4:p.Pro365=
ENST00000378324.6:c.922C= ENSP00000367575.2:p.Pro308=
ENST00000403558.1:c.1207C= ENSP00000384420.1:p.Pro403=
ENST00000528996.1:c.279C= ENSP00000431226.1:n.279C=
ENST00000530113.1:n.535C=
ENST00000531133.5:c.579C= ENSP00000435431.1:n.579C=
ENST00000531797.5:c.*103C= ENSP00000432554.1:n.*103C=
ENST00000619430.1:c.349-140C= ENSP00000478572.1:n.349-140C=
NM_000062.2:c.1078C= , LRG_105t1:c.1078C= NP_000053.2:p.Pro360=
NM_001032295.1:c.1078C= NP_001027466.1:p.Pro360=
NM_000062.3:c.1078C= MANE Select NP_000053.2:p.Pro360=
NM_001032295.2:c.1078C= NP_001027466.1:p.Pro360=