Canonical Allele Identifier: CA1975539540
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57614739G= , CM000673.2:g.57614739G= GRCh38
NC_000011.9:g.57382212G= , CM000673.1:g.57382212G= GRCh37
NC_000011.8:g.57138788G= NCBI36
NG_009625.1:g.22186G= , LRG_105:g.22186G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.*158G= MANE Select ENSP00000278407.4:n.*158G=
ENST00000528996.2:c.*558G= ENSP00000431226.2:n.*558G=
ENST00000531605.2:c.*1437G= ENSP00000503752.1:n.*1437G=
ENST00000619430.2:c.*158G= ENSP00000478572.2:n.*158G=
ENST00000676670.1:c.*15+143G= ENSP00000504807.1:n.*15+143G=
ENST00000676741.1:n.2743G=
ENST00000677624.1:c.*1081G= ENSP00000503979.1:n.*1081G=
ENST00000677625.1:c.*158G= ENSP00000502857.1:n.*158G=
ENST00000677856.1:n.1914G=
ENST00000677915.1:c.*558G= ENSP00000503118.1:n.*558G=
ENST00000678533.1:c.*1072+143G= ENSP00000503873.1:n.*1072+143G=
ENST00000678592.1:c.*601G= ENSP00000504424.1:n.*601G=
ENST00000278407.8:c.*158G= ENSP00000278407.4:n.*158G=
ENST00000340687.10:c.*158G= ENSP00000341861.6:n.*158G=
ENST00000378323.8:c.*158G= ENSP00000367574.4:n.*158G=
ENST00000378324.6:c.*158G= ENSP00000367575.2:n.*158G=
ENST00000403558.1:c.*158G= ENSP00000384420.1:n.*158G=
ENST00000528996.1:c.862G= ENSP00000431226.1:n.862G=
ENST00000531797.5:c.*686G= ENSP00000432554.1:n.*686G=
NM_000062.2:c.*158G= , LRG_105t1:c.*158G= NP_000053.2:n.*158G=
NM_001032295.1:c.*158G= NP_001027466.1:n.*158G=
NM_000062.3:c.*158G= MANE Select NP_000053.2:n.*158G=
NM_001032295.2:c.*158G= NP_001027466.1:n.*158G=