Canonical Allele Identifier: CA2574828305
Gene: SERPING1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57614632C>T , CM000673.2:g.57614632C>T GRCh38
NC_000011.9:g.57382105C>T , CM000673.1:g.57382105C>T GRCh37
NC_000011.8:g.57138681C>T NCBI36
NG_009625.1:g.22079C>T , LRG_105:g.22079C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.*51C>T MANE Select ENSP00000278407.4:n.*51C>T
ENST00000528996.2:c.*451C>T ENSP00000431226.2:n.*451C>T
ENST00000531605.2:c.*1330C>T ENSP00000503752.1:n.*1330C>T
ENST00000619430.2:c.*51C>T ENSP00000478572.2:n.*51C>T
ENST00000676670.1:c.*15+36C>T ENSP00000504807.1:n.*15+36C>T
ENST00000676741.1:n.2636C>T
ENST00000677624.1:c.*974C>T ENSP00000503979.1:n.*974C>T
ENST00000677625.1:c.*51C>T ENSP00000502857.1:n.*51C>T
ENST00000677856.1:n.1807C>T
ENST00000677915.1:c.*451C>T ENSP00000503118.1:n.*451C>T
ENST00000678533.1:c.*1072+36C>T ENSP00000503873.1:n.*1072+36C>T
ENST00000678592.1:c.*494C>T ENSP00000504424.1:n.*494C>T
ENST00000278407.8:c.*51C>T ENSP00000278407.4:n.*51C>T
ENST00000340687.10:c.*51C>T ENSP00000341861.6:n.*51C>T
ENST00000378323.8:c.*51C>T ENSP00000367574.4:n.*51C>T
ENST00000378324.6:c.*51C>T ENSP00000367575.2:n.*51C>T
ENST00000403558.1:c.*51C>T ENSP00000384420.1:n.*51C>T
ENST00000528996.1:c.755C>T ENSP00000431226.1:n.755C>T
ENST00000531797.5:c.*579C>T ENSP00000432554.1:n.*579C>T
NM_000062.2:c.*51C>T , LRG_105t1:c.*51C>T NP_000053.2:n.*51C>T
NM_001032295.1:c.*51C>T NP_001027466.1:n.*51C>T
NM_000062.3:c.*51C>T MANE Select NP_000053.2:n.*51C>T
NM_001032295.2:c.*51C>T NP_001027466.1:n.*51C>T