Canonical Allele Identifier: CA380702565
Gene: SERPING1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57611768C>G , CM000673.2:g.57611768C>G GRCh38
NC_000011.9:g.57379241C>G , CM000673.1:g.57379241C>G GRCh37
NC_000011.8:g.57135817C>G NCBI36
NG_009625.1:g.19215C>G , LRG_105:g.19215C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000278407.9:c.1081C>G MANE Select ENSP00000278407.4:p.Gln361Glu
ENST00000528996.2:c.101C>G ENSP00000431226.2:p.Pro34Arg
ENST00000531605.2:c.*857C>G ENSP00000503752.1:n.*857C>G
ENST00000619430.2:c.877C>G ENSP00000478572.2:p.Gln293Glu
ENST00000676670.1:c.1081C>G ENSP00000504807.1:p.Gln361Glu
ENST00000676741.1:n.2163C>G
ENST00000677624.1:c.*501C>G ENSP00000503979.1:n.*501C>G
ENST00000677625.1:c.1030-3C>G ENSP00000502857.1:n.1030-3C>G
ENST00000677856.1:n.1334C>G
ENST00000677915.1:c.737C>G ENSP00000503118.1:p.Pro246Arg
ENST00000678533.1:c.*635C>G ENSP00000503873.1:n.*635C>G
ENST00000678592.1:c.*21C>G ENSP00000504424.1:n.*21C>G
ENST00000278407.8:c.1081C>G ENSP00000278407.4:p.Gln361Glu
ENST00000340687.10:c.1030-60C>G ENSP00000341861.6:n.1030-60C>G
ENST00000378323.8:c.1096C>G ENSP00000367574.4:p.Gln366Glu
ENST00000378324.6:c.925C>G ENSP00000367575.2:p.Gln309Glu
ENST00000403558.1:c.1210C>G ENSP00000384420.1:p.Gln404Glu
ENST00000528996.1:c.282C>G ENSP00000431226.1:n.282C>G
ENST00000530113.1:n.538C>G
ENST00000531133.5:c.582C>G ENSP00000435431.1:n.582C>G
ENST00000531797.5:c.*106C>G ENSP00000432554.1:n.*106C>G
ENST00000619430.1:c.349-137C>G ENSP00000478572.1:n.349-137C>G
NM_000062.2:c.1081C>G , LRG_105t1:c.1081C>G NP_000053.2:p.Gln361Glu
NM_001032295.1:c.1081C>G NP_001027466.1:p.Gln361Glu
NM_000062.3:c.1081C>G MANE Select NP_000053.2:p.Gln361Glu
NM_001032295.2:c.1081C>G NP_001027466.1:p.Gln361Glu