Canonical Allele Identifier: CA1975539369
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57614575G= , CM000673.2:g.57614575G= GRCh38
NC_000011.9:g.57382048G= , CM000673.1:g.57382048G= GRCh37
NC_000011.8:g.57138624G= NCBI36
NG_009625.1:g.22022G= , LRG_105:g.22022G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.1497G= MANE Select ENSP00000278407.4:p.Arg499=
ENST00000528996.2:c.*394G= ENSP00000431226.2:n.*394G=
ENST00000531605.2:c.*1273G= ENSP00000503752.1:n.*1273G=
ENST00000619430.2:c.1293G= ENSP00000478572.2:p.Arg431=
ENST00000676670.1:c.1497G= ENSP00000504807.1:p.Arg499=
ENST00000676741.1:n.2579G=
ENST00000677624.1:c.*917G= ENSP00000503979.1:n.*917G=
ENST00000677625.1:c.1443G= ENSP00000502857.1:p.Arg481=
ENST00000677856.1:n.1750G=
ENST00000677915.1:c.*394G= ENSP00000503118.1:n.*394G=
ENST00000678533.1:c.*1051G= ENSP00000503873.1:n.*1051G=
ENST00000678592.1:c.*437G= ENSP00000504424.1:n.*437G=
ENST00000278407.8:c.1497G= ENSP00000278407.4:p.Arg499=
ENST00000340687.10:c.1386G= ENSP00000341861.6:p.Arg462=
ENST00000378323.8:c.1512G= ENSP00000367574.4:p.Arg504=
ENST00000378324.6:c.1341G= ENSP00000367575.2:p.Arg447=
ENST00000403558.1:c.1626G= ENSP00000384420.1:p.Arg542=
ENST00000528996.1:c.698G= ENSP00000431226.1:n.698G=
ENST00000531133.5:c.998G= ENSP00000435431.1:n.998G=
ENST00000531797.5:c.*522G= ENSP00000432554.1:n.*522G=
ENST00000619430.1:c.628G= ENSP00000478572.1:n.628G=
NM_000062.2:c.1497G= , LRG_105t1:c.1497G= NP_000053.2:p.Arg499=
NM_001032295.1:c.1497G= NP_001027466.1:p.Arg499=
NM_000062.3:c.1497G= MANE Select NP_000053.2:p.Arg499=
NM_001032295.2:c.1497G= NP_001027466.1:p.Arg499=