Canonical Allele Identifier: CA1975539440
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57614641C= , CM000673.2:g.57614641C= GRCh38
NC_000011.9:g.57382114C= , CM000673.1:g.57382114C= GRCh37
NC_000011.8:g.57138690C= NCBI36
NG_009625.1:g.22088C= , LRG_105:g.22088C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.*60C= MANE Select ENSP00000278407.4:n.*60C=
ENST00000528996.2:c.*460C= ENSP00000431226.2:n.*460C=
ENST00000531605.2:c.*1339C= ENSP00000503752.1:n.*1339C=
ENST00000619430.2:c.*60C= ENSP00000478572.2:n.*60C=
ENST00000676670.1:c.*15+45C= ENSP00000504807.1:n.*15+45C=
ENST00000676741.1:n.2645C=
ENST00000677624.1:c.*983C= ENSP00000503979.1:n.*983C=
ENST00000677625.1:c.*60C= ENSP00000502857.1:n.*60C=
ENST00000677856.1:n.1816C=
ENST00000677915.1:c.*460C= ENSP00000503118.1:n.*460C=
ENST00000678533.1:c.*1072+45C= ENSP00000503873.1:n.*1072+45C=
ENST00000678592.1:c.*503C= ENSP00000504424.1:n.*503C=
ENST00000278407.8:c.*60C= ENSP00000278407.4:n.*60C=
ENST00000340687.10:c.*60C= ENSP00000341861.6:n.*60C=
ENST00000378323.8:c.*60C= ENSP00000367574.4:n.*60C=
ENST00000378324.6:c.*60C= ENSP00000367575.2:n.*60C=
ENST00000403558.1:c.*60C= ENSP00000384420.1:n.*60C=
ENST00000528996.1:c.764C= ENSP00000431226.1:n.764C=
ENST00000531797.5:c.*588C= ENSP00000432554.1:n.*588C=
NM_000062.2:c.*60C= , LRG_105t1:c.*60C= NP_000053.2:n.*60C=
NM_001032295.1:c.*60C= NP_001027466.1:n.*60C=
NM_000062.3:c.*60C= MANE Select NP_000053.2:n.*60C=
NM_001032295.2:c.*60C= NP_001027466.1:n.*60C=