Canonical Allele Identifier: CA1975539207
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57614458C= , CM000673.2:g.57614458C= GRCh38
NC_000011.9:g.57381931C= , CM000673.1:g.57381931C= GRCh37
NC_000011.8:g.57138507C= NCBI36
NG_009625.1:g.21905C= , LRG_105:g.21905C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.1380C= MANE Select ENSP00000278407.4:p.Ser460=
ENST00000528996.2:c.*277C= ENSP00000431226.2:n.*277C=
ENST00000531605.2:c.*1156C= ENSP00000503752.1:n.*1156C=
ENST00000619430.2:c.1176C= ENSP00000478572.2:p.Ser392=
ENST00000676670.1:c.1380C= ENSP00000504807.1:p.Ser460=
ENST00000676741.1:n.2462C=
ENST00000677624.1:c.*800C= ENSP00000503979.1:n.*800C=
ENST00000677625.1:c.1326C= ENSP00000502857.1:p.Ser442=
ENST00000677856.1:n.1633C=
ENST00000677915.1:c.*277C= ENSP00000503118.1:n.*277C=
ENST00000678533.1:c.*934C= ENSP00000503873.1:n.*934C=
ENST00000678592.1:c.*320C= ENSP00000504424.1:n.*320C=
ENST00000278407.8:c.1380C= ENSP00000278407.4:p.Ser460=
ENST00000340687.10:c.1269C= ENSP00000341861.6:p.Ser423=
ENST00000378323.8:c.1395C= ENSP00000367574.4:p.Ser465=
ENST00000378324.6:c.1224C= ENSP00000367575.2:p.Ser408=
ENST00000403558.1:c.1509C= ENSP00000384420.1:p.Ser503=
ENST00000528996.1:c.581C= ENSP00000431226.1:n.581C=
ENST00000530113.1:n.837C=
ENST00000531133.5:c.881C= ENSP00000435431.1:n.881C=
ENST00000531797.5:c.*405C= ENSP00000432554.1:n.*405C=
ENST00000619430.1:c.511C= ENSP00000478572.1:n.511C=
NM_000062.2:c.1380C= , LRG_105t1:c.1380C= NP_000053.2:p.Ser460=
NM_001032295.1:c.1380C= NP_001027466.1:p.Ser460=
NM_000062.3:c.1380C= MANE Select NP_000053.2:p.Ser460=
NM_001032295.2:c.1380C= NP_001027466.1:p.Ser460=