Canonical Allele Identifier: CA2695214133
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57606217_57606221del , CM000673.2:g.57606217_57606221del GRCh38
NC_000011.9:g.57373690_57373694del , CM000673.1:g.57373690_57373694del GRCh37
NC_000011.8:g.57130266_57130270del NCBI36
NG_009625.1:g.13664_13668del , LRG_105:g.13664_13668del

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.889+4_889+8del MANE Select ENSP00000278407.4:n.889+4_889+8del
ENST00000528996.2:c.59-5509_59-5505del ENSP00000431226.2:n.59-5509_59-5505del
ENST00000531605.2:c.*665+4_*665+8del ENSP00000503752.1:n.*665+4_*665+8del
ENST00000619430.2:c.686-191_686-187del ENSP00000478572.2:n.686-191_686-187del
ENST00000676670.1:c.889+4_889+8del ENSP00000504807.1:n.889+4_889+8del
ENST00000676741.1:n.1971+4_1971+8del
ENST00000677624.1:c.*309+4_*309+8del ENSP00000503979.1:n.*309+4_*309+8del
ENST00000677625.1:c.889+4_889+8del ENSP00000502857.1:n.889+4_889+8del
ENST00000677856.1:n.952_956del
ENST00000677915.1:c.685+4048_685+4052del ENSP00000503118.1:n.685+4048_685+4052del
ENST00000678533.1:c.*443+4_*443+8del ENSP00000503873.1:n.*443+4_*443+8del
ENST00000678592.1:c.889+4_889+8del ENSP00000504424.1:n.889+4_889+8del
ENST00000278407.8:c.889+4_889+8del ENSP00000278407.4:n.889+4_889+8del
ENST00000340687.10:c.889+4_889+8del ENSP00000341861.6:n.889+4_889+8del
ENST00000378323.8:c.904+4_904+8del ENSP00000367574.4:n.904+4_904+8del
ENST00000378324.6:c.733+4_733+8del ENSP00000367575.2:n.733+4_733+8del
ENST00000403558.1:c.991+4_991+8del ENSP00000384420.1:n.991+4_991+8del
ENST00000531133.5:c.390+4_390+8del ENSP00000435431.1:n.390+4_390+8del
ENST00000531797.5:c.*54+4048_*54+4052del ENSP00000432554.1:n.*54+4048_*54+4052del
ENST00000619430.1:c.349-5688_349-5684del ENSP00000478572.1:n.349-5688_349-5684del
NM_000062.2:c.889+4_889+8del , LRG_105t1:c.889+4_889+8del NP_000053.2:n.889+4_889+8del
NM_001032295.1:c.889+4_889+8del NP_001027466.1:n.889+4_889+8del
NM_000062.3:c.889+4_889+8del MANE Select NP_000053.2:n.889+4_889+8del
NM_001032295.2:c.889+4_889+8del NP_001027466.1:n.889+4_889+8del