Canonical Allele Identifier: CA1975523444
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57600082_57600106delinsACCCACCACACAACCCACCACAGAG , CM000673.2:g.57600082_57600106delinsACCCACCACACAACCCACCACAGAG GRCh38
NC_000011.9:g.57367555_57367579delinsACCCACCACACAACCCACCACAGAG , CM000673.1:g.57367555_57367579delinsACCCACCACACAACCCACCACAGAG GRCh37
NC_000011.8:g.57124131_57124155delinsACCCACCACACAACCCACCACAGAG NCBI36
NG_009625.1:g.7529_7553delinsACCCACCACACAACCCACCACAGAG , LRG_105:g.7529_7553delinsACCCACCACACAACCCACCACAGAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.255_279delinsACCCACCACACAACCCACCACAGAG MANE Select ENSP00000278407.4:p.Glu85=
ENST00000528996.2:c.58+1754_58+1778delinsACCCACCACACAACCCACCACAGAG ENSP00000431226.2:n.58+1754_58+1778delinsACCCACCACACAACCCACCA...
ENST00000531605.2:c.51+1761_51+1785delinsACCCACCACACAACCCACCACAGAG ENSP00000503752.1:n.51+1761_51+1785delinsACCCACCACACAACCCACCA...
ENST00000619430.2:c.255_279delinsACCCACCACACAACCCACCACAGAG ENSP00000478572.2:p.Glu85=
ENST00000676670.1:c.255_279delinsACCCACCACACAACCCACCACAGAG ENSP00000504807.1:p.Glu85=
ENST00000676741.1:n.1337_1361delinsACCCACCACACAACCCACCACAGAG
ENST00000677275.1:n.242_266delinsACCCACCACACAACCCACCACAGAG
ENST00000677624.1:c.255_279delinsACCCACCACACAACCCACCACAGAG ENSP00000503979.1:p.Glu85=
ENST00000677625.1:c.255_279delinsACCCACCACACAACCCACCACAGAG ENSP00000502857.1:p.Glu85=
ENST00000677856.1:n.314_338delinsACCCACCACACAACCCACCACAGAG
ENST00000677915.1:c.255_279delinsACCCACCACACAACCCACCACAGAG ENSP00000503118.1:p.Glu85=
ENST00000678533.1:c.51+1761_51+1785delinsACCCACCACACAACCCACCACAGAG ENSP00000503873.1:n.51+1761_51+1785delinsACCCACCACACAACCCACCA...
ENST00000678592.1:c.255_279delinsACCCACCACACAACCCACCACAGAG ENSP00000504424.1:p.Glu85=
ENST00000278407.8:c.255_279delinsACCCACCACACAACCCACCACAGAG ENSP00000278407.4:p.Glu85=
ENST00000340687.10:c.255_279delinsACCCACCACACAACCCACCACAGAG ENSP00000341861.6:p.Glu85=
ENST00000378323.8:c.270_294delinsACCCACCACACAACCCACCACAGAG ENSP00000367574.4:p.Glu90=
ENST00000378324.6:c.99_123delinsACCCACCACACAACCCACCACAGAG ENSP00000367575.2:p.Glu33=
ENST00000403558.1:c.357_381delinsACCCACCACACAACCCACCACAGAG ENSP00000384420.1:p.Glu119=
ENST00000405496.5:c.255_279delinsACCCACCACACAACCCACCACAGAG ENSP00000384561.1:p.Glu85=
ENST00000531133.5:c.51+1761_51+1785delinsACCCACCACACAACCCACCACAGAG ENSP00000435431.1:n.51+1761_51+1785delinsACCCACCACACAACCCACCA...
ENST00000531797.5:c.51+1761_51+1785delinsACCCACCACACAACCCACCACAGAG ENSP00000432554.1:n.51+1761_51+1785delinsACCCACCACACAACCCACCA...
ENST00000619430.1:c.255_279delinsACCCACCACACAACCCACCACAGAG ENSP00000478572.1:p.Glu85=
NM_000062.2:c.255_279delinsACCCACCACACAACCCACCACAGAG , LRG_105t1:c.255_279delinsACCCACCACACAACCCACCACAGAG NP_000053.2:p.Glu85=
NM_001032295.1:c.255_279delinsACCCACCACACAACCCACCACAGAG NP_001027466.1:p.Glu85=
NM_000062.3:c.255_279delinsACCCACCACACAACCCACCACAGAG MANE Select NP_000053.2:p.Glu85=
NM_001032295.2:c.255_279delinsACCCACCACACAACCCACCACAGAG NP_001027466.1:p.Glu85=