Canonical Allele Identifier: CA2613603825
Gene: SERPING1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57614707A>C , CM000673.2:g.57614707A>C GRCh38
NC_000011.9:g.57382180A>C , CM000673.1:g.57382180A>C GRCh37
NC_000011.8:g.57138756A>C NCBI36
NG_009625.1:g.22154A>C , LRG_105:g.22154A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.*126A>C MANE Select ENSP00000278407.4:n.*126A>C
ENST00000528996.2:c.*526A>C ENSP00000431226.2:n.*526A>C
ENST00000531605.2:c.*1405A>C ENSP00000503752.1:n.*1405A>C
ENST00000619430.2:c.*126A>C ENSP00000478572.2:n.*126A>C
ENST00000676670.1:c.*15+111A>C ENSP00000504807.1:n.*15+111A>C
ENST00000676741.1:n.2711A>C
ENST00000677624.1:c.*1049A>C ENSP00000503979.1:n.*1049A>C
ENST00000677625.1:c.*126A>C ENSP00000502857.1:n.*126A>C
ENST00000677856.1:n.1882A>C
ENST00000677915.1:c.*526A>C ENSP00000503118.1:n.*526A>C
ENST00000678533.1:c.*1072+111A>C ENSP00000503873.1:n.*1072+111A>C
ENST00000678592.1:c.*569A>C ENSP00000504424.1:n.*569A>C
ENST00000278407.8:c.*126A>C ENSP00000278407.4:n.*126A>C
ENST00000340687.10:c.*126A>C ENSP00000341861.6:n.*126A>C
ENST00000378323.8:c.*126A>C ENSP00000367574.4:n.*126A>C
ENST00000378324.6:c.*126A>C ENSP00000367575.2:n.*126A>C
ENST00000403558.1:c.*126A>C ENSP00000384420.1:n.*126A>C
ENST00000528996.1:c.830A>C ENSP00000431226.1:n.830A>C
ENST00000531797.5:c.*654A>C ENSP00000432554.1:n.*654A>C
NM_000062.2:c.*126A>C , LRG_105t1:c.*126A>C NP_000053.2:n.*126A>C
NM_001032295.1:c.*126A>C NP_001027466.1:n.*126A>C
NM_000062.3:c.*126A>C MANE Select NP_000053.2:n.*126A>C
NM_001032295.2:c.*126A>C NP_001027466.1:n.*126A>C