Canonical Allele Identifier: CA1975522990
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57599768C= , CM000673.2:g.57599768C= GRCh38
NC_000011.9:g.57367241C= , CM000673.1:g.57367241C= GRCh37
NC_000011.8:g.57123817C= NCBI36
NG_009625.1:g.7215C= , LRG_105:g.7215C=

Transcript Alleles

HGVS Amino-acid change
ENST00000278407.9:c.52-111C= MANE Select ENSP00000278407.4:n.52-111C=
ENST00000528996.2:c.58+1440C= ENSP00000431226.2:n.58+1440C=
ENST00000531605.2:c.51+1447C= ENSP00000503752.1:n.51+1447C=
ENST00000619430.2:c.52-111C= ENSP00000478572.2:n.52-111C=
ENST00000676670.1:c.52-111C= ENSP00000504807.1:n.52-111C=
ENST00000676741.1:n.1023C=
ENST00000677275.1:n.39-111C=
ENST00000677624.1:c.52-111C= ENSP00000503979.1:n.52-111C=
ENST00000677625.1:c.52-111C= ENSP00000502857.1:n.52-111C=
ENST00000677856.1:n.111-111C=
ENST00000677915.1:c.52-111C= ENSP00000503118.1:n.52-111C=
ENST00000678533.1:c.51+1447C= ENSP00000503873.1:n.51+1447C=
ENST00000678592.1:c.52-111C= ENSP00000504424.1:n.52-111C=
ENST00000278407.8:c.52-111C= ENSP00000278407.4:n.52-111C=
ENST00000340687.10:c.52-111C= ENSP00000341861.6:n.52-111C=
ENST00000378323.8:c.52-96C= ENSP00000367574.4:n.52-96C=
ENST00000378324.6:c.-105-111C= ENSP00000367575.2:n.-105-111C=
ENST00000403558.1:c.154-111C= ENSP00000384420.1:n.154-111C=
ENST00000405496.5:c.52-111C= ENSP00000384561.1:n.52-111C=
ENST00000457869.1:c.154-111C= ENSP00000399746.1:n.154-111C=
ENST00000531133.5:c.51+1447C= ENSP00000435431.1:n.51+1447C=
ENST00000531797.5:c.51+1447C= ENSP00000432554.1:n.51+1447C=
ENST00000619430.1:c.52-111C= ENSP00000478572.1:n.52-111C=
NM_000062.2:c.52-111C= , LRG_105t1:c.52-111C= NP_000053.2:n.52-111C=
NM_001032295.1:c.52-111C= NP_001027466.1:n.52-111C=
NM_000062.3:c.52-111C= MANE Select NP_000053.2:n.52-111C=
NM_001032295.2:c.52-111C= NP_001027466.1:n.52-111C=