Canonical Allele Identifier: CA1975525902
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57602073C= , CM000673.2:g.57602073C= GRCh38
NC_000011.9:g.57369546C= , CM000673.1:g.57369546C= GRCh37
NC_000011.8:g.57126122C= NCBI36
NG_009625.1:g.9520C= , LRG_105:g.9520C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.589C= MANE Select ENSP00000278407.4:p.Leu197=
ENST00000528996.2:c.58+3745C= ENSP00000431226.2:n.58+3745C=
ENST00000531605.2:c.90C= ENSP00000503752.1:p.Ser30=
ENST00000619430.2:c.589C= ENSP00000478572.2:p.Leu197=
ENST00000676670.1:c.589C= ENSP00000504807.1:p.Leu197=
ENST00000676741.1:n.1671C=
ENST00000677275.1:n.576C=
ENST00000677624.1:c.589C= ENSP00000503979.1:p.Leu197=
ENST00000677625.1:c.589C= ENSP00000502857.1:p.Leu197=
ENST00000677856.1:n.648C=
ENST00000677915.1:c.589C= ENSP00000503118.1:p.Leu197=
ENST00000678533.1:c.90C= ENSP00000503873.1:p.Ser30=
ENST00000678592.1:c.589C= ENSP00000504424.1:p.Leu197=
ENST00000278407.8:c.589C= ENSP00000278407.4:p.Leu197=
ENST00000340687.10:c.589C= ENSP00000341861.6:p.Leu197=
ENST00000378323.8:c.604C= ENSP00000367574.4:p.Leu202=
ENST00000378324.6:c.433C= ENSP00000367575.2:p.Leu145=
ENST00000403558.1:c.691C= ENSP00000384420.1:p.Leu231=
ENST00000531133.5:c.90C= ENSP00000435431.1:p.Ser30=
ENST00000531605.1:n.29C=
ENST00000531797.5:c.90C= ENSP00000432554.1:p.Ser30=
ENST00000619430.1:c.348+1898C= ENSP00000478572.1:n.348+1898C=
NM_000062.2:c.589C= , LRG_105t1:c.589C= NP_000053.2:p.Leu197=
NM_001032295.1:c.589C= NP_001027466.1:p.Leu197=
NM_000062.3:c.589C= MANE Select NP_000053.2:p.Leu197=
NM_001032295.2:c.589C= NP_001027466.1:p.Leu197=