Canonical Allele Identifier: CA2613603363
Gene: SERPING1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57614605G>C , CM000673.2:g.57614605G>C GRCh38
NC_000011.9:g.57382078G>C , CM000673.1:g.57382078G>C GRCh37
NC_000011.8:g.57138654G>C NCBI36
NG_009625.1:g.22052G>C , LRG_105:g.22052G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.*24G>C MANE Select ENSP00000278407.4:n.*24G>C
ENST00000528996.2:c.*424G>C ENSP00000431226.2:n.*424G>C
ENST00000531605.2:c.*1303G>C ENSP00000503752.1:n.*1303G>C
ENST00000619430.2:c.*24G>C ENSP00000478572.2:n.*24G>C
ENST00000676670.1:c.*15+9G>C ENSP00000504807.1:n.*15+9G>C
ENST00000676741.1:n.2609G>C
ENST00000677624.1:c.*947G>C ENSP00000503979.1:n.*947G>C
ENST00000677625.1:c.*24G>C ENSP00000502857.1:n.*24G>C
ENST00000677856.1:n.1780G>C
ENST00000677915.1:c.*424G>C ENSP00000503118.1:n.*424G>C
ENST00000678533.1:c.*1072+9G>C ENSP00000503873.1:n.*1072+9G>C
ENST00000678592.1:c.*467G>C ENSP00000504424.1:n.*467G>C
ENST00000278407.8:c.*24G>C ENSP00000278407.4:n.*24G>C
ENST00000340687.10:c.*24G>C ENSP00000341861.6:n.*24G>C
ENST00000378323.8:c.*24G>C ENSP00000367574.4:n.*24G>C
ENST00000378324.6:c.*24G>C ENSP00000367575.2:n.*24G>C
ENST00000403558.1:c.*24G>C ENSP00000384420.1:n.*24G>C
ENST00000528996.1:c.728G>C ENSP00000431226.1:n.728G>C
ENST00000531797.5:c.*552G>C ENSP00000432554.1:n.*552G>C
NM_000062.2:c.*24G>C , LRG_105t1:c.*24G>C NP_000053.2:n.*24G>C
NM_001032295.1:c.*24G>C NP_001027466.1:n.*24G>C
NM_000062.3:c.*24G>C MANE Select NP_000053.2:n.*24G>C
NM_001032295.2:c.*24G>C NP_001027466.1:n.*24G>C