Canonical Allele Identifier: CA678581188

Gene: SERPING1

Linked Data

• dbSNP Id: rs1179812169
• MyVariant Identifiers: chr11:g.57382157_57382165del (hg19) ; chr11:g.57614684_57614692del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614685_57614693del , CM000673.2:g.57614685_57614693del	GRCh38
NC_000011.9:g.57382158_57382166del , CM000673.1:g.57382158_57382166del	GRCh37
NC_000011.8:g.57138734_57138742del	NCBI36
NG_009625.1:g.22132_22140del , LRG_105:g.22132_22140del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.*104_*112del MANE Select	ENSP00000278407.4:n.*104_*112del
ENST00000528996.2:c.*504_*512del	ENSP00000431226.2:n.*504_*512del
ENST00000531605.2:c.*1383_*1391del	ENSP00000503752.1:n.*1383_*1391del
ENST00000619430.2:c.*104_*112del	ENSP00000478572.2:n.*104_*112del
ENST00000676670.1:c.*15+89_*15+97del	ENSP00000504807.1:n.*15+89_*15+97del
ENST00000676741.1:n.2689_2697del
ENST00000677624.1:c.*1027_*1035del	ENSP00000503979.1:n.*1027_*1035del
ENST00000677625.1:c.*104_*112del	ENSP00000502857.1:n.*104_*112del
ENST00000677856.1:n.1860_1868del
ENST00000677915.1:c.*504_*512del	ENSP00000503118.1:n.*504_*512del
ENST00000678533.1:c.*1072+89_*1072+97del	ENSP00000503873.1:n.*1072+89_*1072+97del
ENST00000678592.1:c.*547_*555del	ENSP00000504424.1:n.*547_*555del
ENST00000278407.8:c.*104_*112del	ENSP00000278407.4:n.*104_*112del
ENST00000340687.10:c.*104_*112del	ENSP00000341861.6:n.*104_*112del
ENST00000378323.8:c.*104_*112del	ENSP00000367574.4:n.*104_*112del
ENST00000378324.6:c.*104_*112del	ENSP00000367575.2:n.*104_*112del
ENST00000403558.1:c.*104_*112del	ENSP00000384420.1:n.*104_*112del
ENST00000528996.1:c.808_816del	ENSP00000431226.1:n.808_816del
ENST00000531797.5:c.*632_*640del	ENSP00000432554.1:n.*632_*640del
NM_000062.2:c.*104_*112del , LRG_105t1:c.*104_*112del	NP_000053.2:n.*104_*112del
NM_001032295.1:c.*104_*112del	NP_001027466.1:n.*104_*112del
NM_000062.3:c.*104_*112del MANE Select	NP_000053.2:n.*104_*112del
NM_001032295.2:c.*104_*112del	NP_001027466.1:n.*104_*112del