Canonical Allele Identifier: CA1975531269
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57606035G= , CM000673.2:g.57606035G= GRCh38
NC_000011.9:g.57373508G= , CM000673.1:g.57373508G= GRCh37
NC_000011.8:g.57130084G= NCBI36
NG_009625.1:g.13482G= , LRG_105:g.13482G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.711G= MANE Select ENSP00000278407.4:p.Val237=
ENST00000528996.2:c.59-5691G= ENSP00000431226.2:n.59-5691G=
ENST00000531605.2:c.*487G= ENSP00000503752.1:n.*487G=
ENST00000619430.2:c.686-373G= ENSP00000478572.2:n.686-373G=
ENST00000676670.1:c.711G= ENSP00000504807.1:p.Val237=
ENST00000676741.1:n.1793G=
ENST00000677624.1:c.*131G= ENSP00000503979.1:n.*131G=
ENST00000677625.1:c.711G= ENSP00000502857.1:p.Val237=
ENST00000677856.1:n.770G=
ENST00000677915.1:c.685+3866G= ENSP00000503118.1:n.685+3866G=
ENST00000678533.1:c.*265G= ENSP00000503873.1:n.*265G=
ENST00000678592.1:c.711G= ENSP00000504424.1:p.Val237=
ENST00000278407.8:c.711G= ENSP00000278407.4:p.Val237=
ENST00000340687.10:c.711G= ENSP00000341861.6:p.Val237=
ENST00000378323.8:c.726G= ENSP00000367574.4:p.Val242=
ENST00000378324.6:c.555G= ENSP00000367575.2:p.Val185=
ENST00000403558.1:c.813G= ENSP00000384420.1:p.Val271=
ENST00000531133.5:c.212G= ENSP00000435431.1:n.212G=
ENST00000531605.1:n.558G=
ENST00000531797.5:c.*54+3866G= ENSP00000432554.1:n.*54+3866G=
ENST00000619430.1:c.348+5860G= ENSP00000478572.1:n.348+5860G=
NM_000062.2:c.711G= , LRG_105t1:c.711G= NP_000053.2:p.Val237=
NM_001032295.1:c.711G= NP_001027466.1:p.Val237=
NM_000062.3:c.711G= MANE Select NP_000053.2:p.Val237=
NM_001032295.2:c.711G= NP_001027466.1:p.Val237=