Canonical Allele Identifier: CA1975531614
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57606209G= , CM000673.2:g.57606209G= GRCh38
NC_000011.9:g.57373682G= , CM000673.1:g.57373682G= GRCh37
NC_000011.8:g.57130258G= NCBI36
NG_009625.1:g.13656G= , LRG_105:g.13656G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.885G= MANE Select ENSP00000278407.4:p.Leu295=
ENST00000528996.2:c.59-5517G= ENSP00000431226.2:n.59-5517G=
ENST00000531605.2:c.*661G= ENSP00000503752.1:n.*661G=
ENST00000619430.2:c.686-199G= ENSP00000478572.2:n.686-199G=
ENST00000676670.1:c.885G= ENSP00000504807.1:p.Leu295=
ENST00000676741.1:n.1967G=
ENST00000677624.1:c.*305G= ENSP00000503979.1:n.*305G=
ENST00000677625.1:c.885G= ENSP00000502857.1:p.Leu295=
ENST00000677856.1:n.944G=
ENST00000677915.1:c.685+4040G= ENSP00000503118.1:n.685+4040G=
ENST00000678533.1:c.*439G= ENSP00000503873.1:n.*439G=
ENST00000678592.1:c.885G= ENSP00000504424.1:p.Leu295=
ENST00000278407.8:c.885G= ENSP00000278407.4:p.Leu295=
ENST00000340687.10:c.885G= ENSP00000341861.6:p.Leu295=
ENST00000378323.8:c.900G= ENSP00000367574.4:p.Leu300=
ENST00000378324.6:c.729G= ENSP00000367575.2:p.Leu243=
ENST00000403558.1:c.987G= ENSP00000384420.1:p.Leu329=
ENST00000531133.5:c.386G= ENSP00000435431.1:n.386G=
ENST00000531797.5:c.*54+4040G= ENSP00000432554.1:n.*54+4040G=
ENST00000619430.1:c.349-5696G= ENSP00000478572.1:n.349-5696G=
NM_000062.2:c.885G= , LRG_105t1:c.885G= NP_000053.2:p.Leu295=
NM_001032295.1:c.885G= NP_001027466.1:p.Leu295=
NM_000062.3:c.885G= MANE Select NP_000053.2:p.Leu295=
NM_001032295.2:c.885G= NP_001027466.1:p.Leu295=