Canonical Allele Identifier: CA2613604039
Gene: SERPING1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57614755C>A , CM000673.2:g.57614755C>A GRCh38
NC_000011.9:g.57382228C>A , CM000673.1:g.57382228C>A GRCh37
NC_000011.8:g.57138804C>A NCBI36
NG_009625.1:g.22202C>A , LRG_105:g.22202C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.*174C>A MANE Select ENSP00000278407.4:n.*174C>A
ENST00000528996.2:c.*574C>A ENSP00000431226.2:n.*574C>A
ENST00000531605.2:c.*1453C>A ENSP00000503752.1:n.*1453C>A
ENST00000619430.2:c.*174C>A ENSP00000478572.2:n.*174C>A
ENST00000676670.1:c.*15+159C>A ENSP00000504807.1:n.*15+159C>A
ENST00000676741.1:n.2759C>A
ENST00000677624.1:c.*1097C>A ENSP00000503979.1:n.*1097C>A
ENST00000677625.1:c.*174C>A ENSP00000502857.1:n.*174C>A
ENST00000677856.1:n.1930C>A
ENST00000677915.1:c.*574C>A ENSP00000503118.1:n.*574C>A
ENST00000678533.1:c.*1072+159C>A ENSP00000503873.1:n.*1072+159C>A
ENST00000678592.1:c.*617C>A ENSP00000504424.1:n.*617C>A
ENST00000278407.8:c.*174C>A ENSP00000278407.4:n.*174C>A
ENST00000340687.10:c.*174C>A ENSP00000341861.6:n.*174C>A
ENST00000378324.6:c.*174C>A ENSP00000367575.2:n.*174C>A
ENST00000403558.1:c.*174C>A ENSP00000384420.1:n.*174C>A
ENST00000528996.1:c.878C>A ENSP00000431226.1:n.878C>A
ENST00000531797.5:c.*702C>A ENSP00000432554.1:n.*702C>A
NM_000062.2:c.*174C>A , LRG_105t1:c.*174C>A NP_000053.2:n.*174C>A
NM_001032295.1:c.*174C>A NP_001027466.1:n.*174C>A
NM_000062.3:c.*174C>A MANE Select NP_000053.2:n.*174C>A
NM_001032295.2:c.*174C>A NP_001027466.1:n.*174C>A