Canonical Allele Identifier: CA1975525917
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57602080A= , CM000673.2:g.57602080A= GRCh38
NC_000011.9:g.57369553A= , CM000673.1:g.57369553A= GRCh37
NC_000011.8:g.57126129A= NCBI36
NG_009625.1:g.9527A= , LRG_105:g.9527A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.596A= MANE Select ENSP00000278407.4:p.Tyr199=
ENST00000528996.2:c.58+3752A= ENSP00000431226.2:n.58+3752A=
ENST00000531605.2:c.97A= ENSP00000503752.1:p.Thr33=
ENST00000619430.2:c.596A= ENSP00000478572.2:p.Tyr199=
ENST00000676670.1:c.596A= ENSP00000504807.1:p.Tyr199=
ENST00000676741.1:n.1678A=
ENST00000677275.1:n.583A=
ENST00000677624.1:c.596A= ENSP00000503979.1:p.Tyr199=
ENST00000677625.1:c.596A= ENSP00000502857.1:p.Tyr199=
ENST00000677856.1:n.655A=
ENST00000677915.1:c.596A= ENSP00000503118.1:p.Tyr199=
ENST00000678533.1:c.97A= ENSP00000503873.1:p.Thr33=
ENST00000678592.1:c.596A= ENSP00000504424.1:p.Tyr199=
ENST00000278407.8:c.596A= ENSP00000278407.4:p.Tyr199=
ENST00000340687.10:c.596A= ENSP00000341861.6:p.Tyr199=
ENST00000378323.8:c.611A= ENSP00000367574.4:p.Tyr204=
ENST00000378324.6:c.440A= ENSP00000367575.2:p.Tyr147=
ENST00000403558.1:c.698A= ENSP00000384420.1:p.Tyr233=
ENST00000531133.5:c.97A= ENSP00000435431.1:p.Thr33=
ENST00000531605.1:n.36A=
ENST00000531797.5:c.97A= ENSP00000432554.1:p.Thr33=
ENST00000619430.1:c.348+1905A= ENSP00000478572.1:n.348+1905A=
NM_000062.2:c.596A= , LRG_105t1:c.596A= NP_000053.2:p.Tyr199=
NM_001032295.1:c.596A= NP_001027466.1:p.Tyr199=
NM_000062.3:c.596A= MANE Select NP_000053.2:p.Tyr199=
NM_001032295.2:c.596A= NP_001027466.1:p.Tyr199=