Canonical Allele Identifier: CA1975539509
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57614702A= , CM000673.2:g.57614702A= GRCh38
NC_000011.9:g.57382175A= , CM000673.1:g.57382175A= GRCh37
NC_000011.8:g.57138751A= NCBI36
NG_009625.1:g.22149A= , LRG_105:g.22149A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.*121A= MANE Select ENSP00000278407.4:n.*121A=
ENST00000528996.2:c.*521A= ENSP00000431226.2:n.*521A=
ENST00000531605.2:c.*1400A= ENSP00000503752.1:n.*1400A=
ENST00000619430.2:c.*121A= ENSP00000478572.2:n.*121A=
ENST00000676670.1:c.*15+106A= ENSP00000504807.1:n.*15+106A=
ENST00000676741.1:n.2706A=
ENST00000677624.1:c.*1044A= ENSP00000503979.1:n.*1044A=
ENST00000677625.1:c.*121A= ENSP00000502857.1:n.*121A=
ENST00000677856.1:n.1877A=
ENST00000677915.1:c.*521A= ENSP00000503118.1:n.*521A=
ENST00000678533.1:c.*1072+106A= ENSP00000503873.1:n.*1072+106A=
ENST00000678592.1:c.*564A= ENSP00000504424.1:n.*564A=
ENST00000278407.8:c.*121A= ENSP00000278407.4:n.*121A=
ENST00000340687.10:c.*121A= ENSP00000341861.6:n.*121A=
ENST00000378323.8:c.*121A= ENSP00000367574.4:n.*121A=
ENST00000378324.6:c.*121A= ENSP00000367575.2:n.*121A=
ENST00000403558.1:c.*121A= ENSP00000384420.1:n.*121A=
ENST00000528996.1:c.825A= ENSP00000431226.1:n.825A=
ENST00000531797.5:c.*649A= ENSP00000432554.1:n.*649A=
NM_000062.2:c.*121A= , LRG_105t1:c.*121A= NP_000053.2:n.*121A=
NM_001032295.1:c.*121A= NP_001027466.1:n.*121A=
NM_000062.3:c.*121A= MANE Select NP_000053.2:n.*121A=
NM_001032295.2:c.*121A= NP_001027466.1:n.*121A=