Canonical Allele Identifier: CA2500829580
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57614722dup , CM000673.2:g.57614722dup GRCh38
NC_000011.9:g.57382195dup , CM000673.1:g.57382195dup GRCh37
NC_000011.8:g.57138771dup NCBI36
NG_009625.1:g.22169dup , LRG_105:g.22169dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.*141dup MANE Select ENSP00000278407.4:n.*141dup
ENST00000528996.2:c.*541dup ENSP00000431226.2:n.*541dup
ENST00000531605.2:c.*1420dup ENSP00000503752.1:n.*1420dup
ENST00000619430.2:c.*141dup ENSP00000478572.2:n.*141dup
ENST00000676670.1:c.*15+126dup ENSP00000504807.1:n.*15+126dup
ENST00000676741.1:n.2726dup
ENST00000677624.1:c.*1064dup ENSP00000503979.1:n.*1064dup
ENST00000677625.1:c.*141dup ENSP00000502857.1:n.*141dup
ENST00000677856.1:n.1897dup
ENST00000677915.1:c.*541dup ENSP00000503118.1:n.*541dup
ENST00000678533.1:c.*1072+126dup ENSP00000503873.1:n.*1072+126dup
ENST00000678592.1:c.*584dup ENSP00000504424.1:n.*584dup
ENST00000278407.8:c.*141dup ENSP00000278407.4:n.*141dup
ENST00000340687.10:c.*141dup ENSP00000341861.6:n.*141dup
ENST00000378323.8:c.*141dup ENSP00000367574.4:n.*141dup
ENST00000378324.6:c.*141dup ENSP00000367575.2:n.*141dup
ENST00000403558.1:c.*141dup ENSP00000384420.1:n.*141dup
ENST00000528996.1:c.845dup ENSP00000431226.1:n.845dup
ENST00000531797.5:c.*669dup ENSP00000432554.1:n.*669dup
NM_000062.2:c.*141dup , LRG_105t1:c.*141dup NP_000053.2:n.*141dup
NM_001032295.1:c.*141dup NP_001027466.1:n.*141dup
NM_000062.3:c.*141dup MANE Select NP_000053.2:n.*141dup
NM_001032295.2:c.*141dup NP_001027466.1:n.*141dup