Canonical Allele Identifier: CA1975539273
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57614487T= , CM000673.2:g.57614487T= GRCh38
NC_000011.9:g.57381960T= , CM000673.1:g.57381960T= GRCh37
NC_000011.8:g.57138536T= NCBI36
NG_009625.1:g.21934T= , LRG_105:g.21934T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.1409T= MANE Select ENSP00000278407.4:p.Val470=
ENST00000528996.2:c.*306T= ENSP00000431226.2:n.*306T=
ENST00000531605.2:c.*1185T= ENSP00000503752.1:n.*1185T=
ENST00000619430.2:c.1205T= ENSP00000478572.2:p.Val402=
ENST00000676670.1:c.1409T= ENSP00000504807.1:p.Val470=
ENST00000676741.1:n.2491T=
ENST00000677624.1:c.*829T= ENSP00000503979.1:n.*829T=
ENST00000677625.1:c.1355T= ENSP00000502857.1:p.Val452=
ENST00000677856.1:n.1662T=
ENST00000677915.1:c.*306T= ENSP00000503118.1:n.*306T=
ENST00000678533.1:c.*963T= ENSP00000503873.1:n.*963T=
ENST00000678592.1:c.*349T= ENSP00000504424.1:n.*349T=
ENST00000278407.8:c.1409T= ENSP00000278407.4:p.Val470=
ENST00000340687.10:c.1298T= ENSP00000341861.6:p.Val433=
ENST00000378323.8:c.1424T= ENSP00000367574.4:p.Val475=
ENST00000378324.6:c.1253T= ENSP00000367575.2:p.Val418=
ENST00000403558.1:c.1538T= ENSP00000384420.1:p.Val513=
ENST00000528996.1:c.610T= ENSP00000431226.1:n.610T=
ENST00000530113.1:n.866T=
ENST00000531133.5:c.910T= ENSP00000435431.1:n.910T=
ENST00000531797.5:c.*434T= ENSP00000432554.1:n.*434T=
ENST00000619430.1:c.540T= ENSP00000478572.1:n.540T=
NM_000062.2:c.1409T= , LRG_105t1:c.1409T= NP_000053.2:p.Val470=
NM_001032295.1:c.1409T= NP_001027466.1:p.Val470=
NM_000062.3:c.1409T= MANE Select NP_000053.2:p.Val470=
NM_001032295.2:c.1409T= NP_001027466.1:p.Val470=