Canonical Allele Identifier: CA599665539

Gene: SERPING1

Linked Data

• dbSNP Id: rs1390634605
• gnomAD v2: 11-57382124-GCCTGCCTGGACTTGGCCCCTGCCACCT-G
• gnomAD v3: 11-57614651-GCCTGCCTGGACTTGGCCCCTGCCACCT-G
• gnomAD v4: 11-57614651-GCCTGCCTGGACTTGGCCCCTGCCACCT-G
• MyVariant Identifiers: chr11:g.57382125_57382151del (hg19) ; chr11:g.57614652_57614678del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614659_57614685del , CM000673.2:g.57614659_57614685del	GRCh38
NC_000011.9:g.57382132_57382158del , CM000673.1:g.57382132_57382158del	GRCh37
NC_000011.8:g.57138708_57138734del	NCBI36
NG_009625.1:g.22106_22132del , LRG_105:g.22106_22132del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.*78_*104del MANE Select	ENSP00000278407.4:n.*78_*104del
ENST00000528996.2:c.*478_*504del	ENSP00000431226.2:n.*478_*504del
ENST00000531605.2:c.*1357_*1383del	ENSP00000503752.1:n.*1357_*1383del
ENST00000619430.2:c.*78_*104del	ENSP00000478572.2:n.*78_*104del
ENST00000676670.1:c.*15+63_*15+89del	ENSP00000504807.1:n.*15+63_*15+89del
ENST00000676741.1:n.2663_2689del
ENST00000677624.1:c.*1001_*1027del	ENSP00000503979.1:n.*1001_*1027del
ENST00000677625.1:c.*78_*104del	ENSP00000502857.1:n.*78_*104del
ENST00000677856.1:n.1834_1860del
ENST00000677915.1:c.*478_*504del	ENSP00000503118.1:n.*478_*504del
ENST00000678533.1:c.*1072+63_*1072+89del	ENSP00000503873.1:n.*1072+63_*1072+89del
ENST00000678592.1:c.*521_*547del	ENSP00000504424.1:n.*521_*547del
ENST00000278407.8:c.*78_*104del	ENSP00000278407.4:n.*78_*104del
ENST00000340687.10:c.*78_*104del	ENSP00000341861.6:n.*78_*104del
ENST00000378323.8:c.*78_*104del	ENSP00000367574.4:n.*78_*104del
ENST00000378324.6:c.*78_*104del	ENSP00000367575.2:n.*78_*104del
ENST00000403558.1:c.*78_*104del	ENSP00000384420.1:n.*78_*104del
ENST00000528996.1:c.782_808del	ENSP00000431226.1:n.782_808del
ENST00000531797.5:c.*606_*632del	ENSP00000432554.1:n.*606_*632del
NM_000062.2:c.*78_*104del , LRG_105t1:c.*78_*104del	NP_000053.2:n.*78_*104del
NM_001032295.1:c.*78_*104del	NP_001027466.1:n.*78_*104del
NM_000062.3:c.*78_*104del MANE Select	NP_000053.2:n.*78_*104del
NM_001032295.2:c.*78_*104del	NP_001027466.1:n.*78_*104del