Canonical Allele Identifier: CA2613603736
Gene: SERPING1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57614684C>A , CM000673.2:g.57614684C>A GRCh38
NC_000011.9:g.57382157C>A , CM000673.1:g.57382157C>A GRCh37
NC_000011.8:g.57138733C>A NCBI36
NG_009625.1:g.22131C>A , LRG_105:g.22131C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.*103C>A MANE Select ENSP00000278407.4:n.*103C>A
ENST00000528996.2:c.*503C>A ENSP00000431226.2:n.*503C>A
ENST00000531605.2:c.*1382C>A ENSP00000503752.1:n.*1382C>A
ENST00000619430.2:c.*103C>A ENSP00000478572.2:n.*103C>A
ENST00000676670.1:c.*15+88C>A ENSP00000504807.1:n.*15+88C>A
ENST00000676741.1:n.2688C>A
ENST00000677624.1:c.*1026C>A ENSP00000503979.1:n.*1026C>A
ENST00000677625.1:c.*103C>A ENSP00000502857.1:n.*103C>A
ENST00000677856.1:n.1859C>A
ENST00000677915.1:c.*503C>A ENSP00000503118.1:n.*503C>A
ENST00000678533.1:c.*1072+88C>A ENSP00000503873.1:n.*1072+88C>A
ENST00000678592.1:c.*546C>A ENSP00000504424.1:n.*546C>A
ENST00000278407.8:c.*103C>A ENSP00000278407.4:n.*103C>A
ENST00000340687.10:c.*103C>A ENSP00000341861.6:n.*103C>A
ENST00000378323.8:c.*103C>A ENSP00000367574.4:n.*103C>A
ENST00000378324.6:c.*103C>A ENSP00000367575.2:n.*103C>A
ENST00000403558.1:c.*103C>A ENSP00000384420.1:n.*103C>A
ENST00000528996.1:c.807C>A ENSP00000431226.1:n.807C>A
ENST00000531797.5:c.*631C>A ENSP00000432554.1:n.*631C>A
NM_000062.2:c.*103C>A , LRG_105t1:c.*103C>A NP_000053.2:n.*103C>A
NM_001032295.1:c.*103C>A NP_001027466.1:n.*103C>A
NM_000062.3:c.*103C>A MANE Select NP_000053.2:n.*103C>A
NM_001032295.2:c.*103C>A NP_001027466.1:n.*103C>A