Canonical Allele Identifier: CA1975539270
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57614486G= , CM000673.2:g.57614486G= GRCh38
NC_000011.9:g.57381959G= , CM000673.1:g.57381959G= GRCh37
NC_000011.8:g.57138535G= NCBI36
NG_009625.1:g.21933G= , LRG_105:g.21933G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.1408G= MANE Select ENSP00000278407.4:p.Val470=
ENST00000528996.2:c.*305G= ENSP00000431226.2:n.*305G=
ENST00000531605.2:c.*1184G= ENSP00000503752.1:n.*1184G=
ENST00000619430.2:c.1204G= ENSP00000478572.2:p.Val402=
ENST00000676670.1:c.1408G= ENSP00000504807.1:p.Val470=
ENST00000676741.1:n.2490G=
ENST00000677624.1:c.*828G= ENSP00000503979.1:n.*828G=
ENST00000677625.1:c.1354G= ENSP00000502857.1:p.Val452=
ENST00000677856.1:n.1661G=
ENST00000677915.1:c.*305G= ENSP00000503118.1:n.*305G=
ENST00000678533.1:c.*962G= ENSP00000503873.1:n.*962G=
ENST00000678592.1:c.*348G= ENSP00000504424.1:n.*348G=
ENST00000278407.8:c.1408G= ENSP00000278407.4:p.Val470=
ENST00000340687.10:c.1297G= ENSP00000341861.6:p.Val433=
ENST00000378323.8:c.1423G= ENSP00000367574.4:p.Val475=
ENST00000378324.6:c.1252G= ENSP00000367575.2:p.Val418=
ENST00000403558.1:c.1537G= ENSP00000384420.1:p.Val513=
ENST00000528996.1:c.609G= ENSP00000431226.1:n.609G=
ENST00000530113.1:n.865G=
ENST00000531133.5:c.909G= ENSP00000435431.1:n.909G=
ENST00000531797.5:c.*433G= ENSP00000432554.1:n.*433G=
ENST00000619430.1:c.539G= ENSP00000478572.1:n.539G=
NM_000062.2:c.1408G= , LRG_105t1:c.1408G= NP_000053.2:p.Val470=
NM_001032295.1:c.1408G= NP_001027466.1:p.Val470=
NM_000062.3:c.1408G= MANE Select NP_000053.2:p.Val470=
NM_001032295.2:c.1408G= NP_001027466.1:p.Val470=