Canonical Allele Identifier: CA2613603593
Gene: SERPING1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57614649C>T , CM000673.2:g.57614649C>T GRCh38
NC_000011.9:g.57382122C>T , CM000673.1:g.57382122C>T GRCh37
NC_000011.8:g.57138698C>T NCBI36
NG_009625.1:g.22096C>T , LRG_105:g.22096C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.*68C>T MANE Select ENSP00000278407.4:n.*68C>T
ENST00000528996.2:c.*468C>T ENSP00000431226.2:n.*468C>T
ENST00000531605.2:c.*1347C>T ENSP00000503752.1:n.*1347C>T
ENST00000619430.2:c.*68C>T ENSP00000478572.2:n.*68C>T
ENST00000676670.1:c.*15+53C>T ENSP00000504807.1:n.*15+53C>T
ENST00000676741.1:n.2653C>T
ENST00000677624.1:c.*991C>T ENSP00000503979.1:n.*991C>T
ENST00000677625.1:c.*68C>T ENSP00000502857.1:n.*68C>T
ENST00000677856.1:n.1824C>T
ENST00000677915.1:c.*468C>T ENSP00000503118.1:n.*468C>T
ENST00000678533.1:c.*1072+53C>T ENSP00000503873.1:n.*1072+53C>T
ENST00000678592.1:c.*511C>T ENSP00000504424.1:n.*511C>T
ENST00000278407.8:c.*68C>T ENSP00000278407.4:n.*68C>T
ENST00000340687.10:c.*68C>T ENSP00000341861.6:n.*68C>T
ENST00000378323.8:c.*68C>T ENSP00000367574.4:n.*68C>T
ENST00000378324.6:c.*68C>T ENSP00000367575.2:n.*68C>T
ENST00000403558.1:c.*68C>T ENSP00000384420.1:n.*68C>T
ENST00000528996.1:c.772C>T ENSP00000431226.1:n.772C>T
ENST00000531797.5:c.*596C>T ENSP00000432554.1:n.*596C>T
NM_000062.2:c.*68C>T , LRG_105t1:c.*68C>T NP_000053.2:n.*68C>T
NM_001032295.1:c.*68C>T NP_001027466.1:n.*68C>T
NM_000062.3:c.*68C>T MANE Select NP_000053.2:n.*68C>T
NM_001032295.2:c.*68C>T NP_001027466.1:n.*68C>T