Canonical Allele Identifier: CA2792229585
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57600111_57600128del , CM000673.2:g.57600111_57600128del GRCh38
NC_000011.9:g.57367584_57367601del , CM000673.1:g.57367584_57367601del GRCh37
NC_000011.8:g.57124160_57124177del NCBI36
NG_009625.1:g.7558_7575del , LRG_105:g.7558_7575del

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.284_301del MANE Select ENSP00000278407.4:p.Thr95_Gln101delinsLys
ENST00000528996.2:c.58+1783_58+1800del ENSP00000431226.2:n.58+1783_58+1800del
ENST00000531605.2:c.51+1790_51+1807del ENSP00000503752.1:n.51+1790_51+1807del
ENST00000619430.2:c.284_301del ENSP00000478572.2:p.Thr95_Gln101delinsLys
ENST00000676670.1:c.284_301del ENSP00000504807.1:p.Thr95_Gln101delinsLys
ENST00000676741.1:n.1366_1383del
ENST00000677275.1:n.271_288del
ENST00000677624.1:c.284_301del ENSP00000503979.1:p.Thr95_Gln101delinsLys
ENST00000677625.1:c.284_301del ENSP00000502857.1:p.Thr95_Gln101delinsLys
ENST00000677856.1:n.343_360del
ENST00000677915.1:c.284_301del ENSP00000503118.1:p.Thr95_Gln101delinsLys
ENST00000678533.1:c.51+1790_51+1807del ENSP00000503873.1:n.51+1790_51+1807del
ENST00000678592.1:c.284_301del ENSP00000504424.1:p.Thr95_Gln101delinsLys
ENST00000278407.8:c.284_301del ENSP00000278407.4:p.Thr95_Gln101delinsLys
ENST00000340687.10:c.284_301del ENSP00000341861.6:p.Thr95_Gln101delinsLys
ENST00000378323.8:c.299_316del ENSP00000367574.4:p.Thr100_Gln106delinsLys
ENST00000378324.6:c.128_145del ENSP00000367575.2:p.Thr43_Gln49delinsLys
ENST00000403558.1:c.386_403del ENSP00000384420.1:p.Thr129_Gln135delinsLys
ENST00000405496.5:c.284_301del ENSP00000384561.1:p.Thr95_Gln101delinsLys
ENST00000531133.5:c.51+1790_51+1807del ENSP00000435431.1:n.51+1790_51+1807del
ENST00000531797.5:c.51+1790_51+1807del ENSP00000432554.1:n.51+1790_51+1807del
ENST00000619430.1:c.284_301del ENSP00000478572.1:p.Thr95_Gln101delinsLys
NM_000062.2:c.284_301del , LRG_105t1:c.284_301del NP_000053.2:p.Thr95_Gln101delinsLys
NM_001032295.1:c.284_301del NP_001027466.1:p.Thr95_Gln101delinsLys
NM_000062.3:c.284_301del MANE Select NP_000053.2:p.Thr95_Gln101delinsLys
NM_001032295.2:c.284_301del NP_001027466.1:p.Thr95_Gln101delinsLys