Canonical Allele Identifier: CA1975536901
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57611766C= , CM000673.2:g.57611766C= GRCh38
NC_000011.9:g.57379239C= , CM000673.1:g.57379239C= GRCh37
NC_000011.8:g.57135815C= NCBI36
NG_009625.1:g.19213C= , LRG_105:g.19213C=

Transcript Alleles

HGVS Amino-acid change
ENST00000278407.9:c.1079C= MANE Select ENSP00000278407.4:p.Pro360=
ENST00000528996.2:c.99C= ENSP00000431226.2:p.Thr33=
ENST00000531605.2:c.*855C= ENSP00000503752.1:n.*855C=
ENST00000619430.2:c.875C= ENSP00000478572.2:p.Pro292=
ENST00000676670.1:c.1079C= ENSP00000504807.1:p.Pro360=
ENST00000676741.1:n.2161C=
ENST00000677624.1:c.*499C= ENSP00000503979.1:n.*499C=
ENST00000677625.1:c.1030-5C= ENSP00000502857.1:n.1030-5C=
ENST00000677856.1:n.1332C=
ENST00000677915.1:c.735C= ENSP00000503118.1:p.Thr245=
ENST00000678533.1:c.*633C= ENSP00000503873.1:n.*633C=
ENST00000678592.1:c.*19C= ENSP00000504424.1:n.*19C=
ENST00000278407.8:c.1079C= ENSP00000278407.4:p.Pro360=
ENST00000340687.10:c.1030-62C= ENSP00000341861.6:n.1030-62C=
ENST00000378323.8:c.1094C= ENSP00000367574.4:p.Pro365=
ENST00000378324.6:c.923C= ENSP00000367575.2:p.Pro308=
ENST00000403558.1:c.1208C= ENSP00000384420.1:p.Pro403=
ENST00000528996.1:c.280C= ENSP00000431226.1:n.280C=
ENST00000530113.1:n.536C=
ENST00000531133.5:c.580C= ENSP00000435431.1:n.580C=
ENST00000531797.5:c.*104C= ENSP00000432554.1:n.*104C=
ENST00000619430.1:c.349-139C= ENSP00000478572.1:n.349-139C=
NM_000062.2:c.1079C= , LRG_105t1:c.1079C= NP_000053.2:p.Pro360=
NM_001032295.1:c.1079C= NP_001027466.1:p.Pro360=
NM_000062.3:c.1079C= MANE Select NP_000053.2:p.Pro360=
NM_001032295.2:c.1079C= NP_001027466.1:p.Pro360=