Canonical Allele Identifier: CA1975539432
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57614638C= , CM000673.2:g.57614638C= GRCh38
NC_000011.9:g.57382111C= , CM000673.1:g.57382111C= GRCh37
NC_000011.8:g.57138687C= NCBI36
NG_009625.1:g.22085C= , LRG_105:g.22085C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.*57C= MANE Select ENSP00000278407.4:n.*57C=
ENST00000528996.2:c.*457C= ENSP00000431226.2:n.*457C=
ENST00000531605.2:c.*1336C= ENSP00000503752.1:n.*1336C=
ENST00000619430.2:c.*57C= ENSP00000478572.2:n.*57C=
ENST00000676670.1:c.*15+42C= ENSP00000504807.1:n.*15+42C=
ENST00000676741.1:n.2642C=
ENST00000677624.1:c.*980C= ENSP00000503979.1:n.*980C=
ENST00000677625.1:c.*57C= ENSP00000502857.1:n.*57C=
ENST00000677856.1:n.1813C=
ENST00000677915.1:c.*457C= ENSP00000503118.1:n.*457C=
ENST00000678533.1:c.*1072+42C= ENSP00000503873.1:n.*1072+42C=
ENST00000678592.1:c.*500C= ENSP00000504424.1:n.*500C=
ENST00000278407.8:c.*57C= ENSP00000278407.4:n.*57C=
ENST00000340687.10:c.*57C= ENSP00000341861.6:n.*57C=
ENST00000378323.8:c.*57C= ENSP00000367574.4:n.*57C=
ENST00000378324.6:c.*57C= ENSP00000367575.2:n.*57C=
ENST00000403558.1:c.*57C= ENSP00000384420.1:n.*57C=
ENST00000528996.1:c.761C= ENSP00000431226.1:n.761C=
ENST00000531797.5:c.*585C= ENSP00000432554.1:n.*585C=
NM_000062.2:c.*57C= , LRG_105t1:c.*57C= NP_000053.2:n.*57C=
NM_001032295.1:c.*57C= NP_001027466.1:n.*57C=
NM_000062.3:c.*57C= MANE Select NP_000053.2:n.*57C=
NM_001032295.2:c.*57C= NP_001027466.1:n.*57C=