Canonical Allele Identifier: CA1975539264
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57614484T= , CM000673.2:g.57614484T= GRCh38
NC_000011.9:g.57381957T= , CM000673.1:g.57381957T= GRCh37
NC_000011.8:g.57138533T= NCBI36
NG_009625.1:g.21931T= , LRG_105:g.21931T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.1406T= MANE Select ENSP00000278407.4:p.Leu469=
ENST00000528996.2:c.*303T= ENSP00000431226.2:n.*303T=
ENST00000531605.2:c.*1182T= ENSP00000503752.1:n.*1182T=
ENST00000619430.2:c.1202T= ENSP00000478572.2:p.Leu401=
ENST00000676670.1:c.1406T= ENSP00000504807.1:p.Leu469=
ENST00000676741.1:n.2488T=
ENST00000677624.1:c.*826T= ENSP00000503979.1:n.*826T=
ENST00000677625.1:c.1352T= ENSP00000502857.1:p.Leu451=
ENST00000677856.1:n.1659T=
ENST00000677915.1:c.*303T= ENSP00000503118.1:n.*303T=
ENST00000678533.1:c.*960T= ENSP00000503873.1:n.*960T=
ENST00000678592.1:c.*346T= ENSP00000504424.1:n.*346T=
ENST00000278407.8:c.1406T= ENSP00000278407.4:p.Leu469=
ENST00000340687.10:c.1295T= ENSP00000341861.6:p.Leu432=
ENST00000378323.8:c.1421T= ENSP00000367574.4:p.Leu474=
ENST00000378324.6:c.1250T= ENSP00000367575.2:p.Leu417=
ENST00000403558.1:c.1535T= ENSP00000384420.1:p.Leu512=
ENST00000528996.1:c.607T= ENSP00000431226.1:n.607T=
ENST00000530113.1:n.863T=
ENST00000531133.5:c.907T= ENSP00000435431.1:n.907T=
ENST00000531797.5:c.*431T= ENSP00000432554.1:n.*431T=
ENST00000619430.1:c.537T= ENSP00000478572.1:n.537T=
NM_000062.2:c.1406T= , LRG_105t1:c.1406T= NP_000053.2:p.Leu469=
NM_001032295.1:c.1406T= NP_001027466.1:p.Leu469=
NM_000062.3:c.1406T= MANE Select NP_000053.2:p.Leu469=
NM_001032295.2:c.1406T= NP_001027466.1:p.Leu469=