Canonical Allele Identifier: CA380702829
Gene: SERPING1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57611807C>A , CM000673.2:g.57611807C>A GRCh38
NC_000011.9:g.57379280C>A , CM000673.1:g.57379280C>A GRCh37
NC_000011.8:g.57135856C>A NCBI36
NG_009625.1:g.19254C>A , LRG_105:g.19254C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.1120C>A MANE Select ENSP00000278407.4:p.Leu374Ile
ENST00000528996.2:c.*17C>A ENSP00000431226.2:n.*17C>A
ENST00000531605.2:c.*896C>A ENSP00000503752.1:n.*896C>A
ENST00000619430.2:c.916C>A ENSP00000478572.2:p.Leu306Ile
ENST00000676670.1:c.1120C>A ENSP00000504807.1:p.Leu374Ile
ENST00000676741.1:n.2202C>A
ENST00000677624.1:c.*540C>A ENSP00000503979.1:n.*540C>A
ENST00000677625.1:c.1066C>A ENSP00000502857.1:p.Leu356Ile
ENST00000677856.1:n.1373C>A
ENST00000677915.1:c.*17C>A ENSP00000503118.1:n.*17C>A
ENST00000678533.1:c.*674C>A ENSP00000503873.1:n.*674C>A
ENST00000678592.1:c.*60C>A ENSP00000504424.1:n.*60C>A
ENST00000278407.8:c.1120C>A ENSP00000278407.4:p.Leu374Ile
ENST00000340687.10:c.1030-21C>A ENSP00000341861.6:n.1030-21C>A
ENST00000378323.8:c.1135C>A ENSP00000367574.4:p.Leu379Ile
ENST00000378324.6:c.964C>A ENSP00000367575.2:p.Leu322Ile
ENST00000403558.1:c.1249C>A ENSP00000384420.1:p.Leu417Ile
ENST00000528996.1:c.321C>A ENSP00000431226.1:n.321C>A
ENST00000530113.1:n.577C>A
ENST00000531133.5:c.621C>A ENSP00000435431.1:n.621C>A
ENST00000531797.5:c.*145C>A ENSP00000432554.1:n.*145C>A
ENST00000619430.1:c.349-98C>A ENSP00000478572.1:n.349-98C>A
NM_000062.2:c.1120C>A , LRG_105t1:c.1120C>A NP_000053.2:p.Leu374Ile
NM_001032295.1:c.1120C>A NP_001027466.1:p.Leu374Ile
NM_000062.3:c.1120C>A MANE Select NP_000053.2:p.Leu374Ile
NM_001032295.2:c.1120C>A NP_001027466.1:p.Leu374Ile