Canonical Allele Identifier: CA599806079

Gene: SERPING1

Linked Data

• dbSNP Id: rs1565173997
• gnomAD v2: 11-57381778-GT-G
• gnomAD v4: 11-57614305-GT-G
• MyVariant Identifiers: chr11:g.57381779del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614310del , CM000673.2:g.57614310del	GRCh38
NC_000011.9:g.57381783del , CM000673.1:g.57381783del	GRCh37
NC_000011.8:g.57138359del	NCBI36
NG_009625.1:g.21757del , LRG_105:g.21757del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1250-18del MANE Select	ENSP00000278407.4:n.1250-18del
ENST00000528996.2:c.*147-18del	ENSP00000431226.2:n.*147-18del
ENST00000531605.2:c.*1026-18del	ENSP00000503752.1:n.*1026-18del
ENST00000619430.2:c.1046-18del	ENSP00000478572.2:n.1046-18del
ENST00000676670.1:c.1250-18del	ENSP00000504807.1:n.1250-18del
ENST00000676741.1:n.2332-18del
ENST00000677624.1:c.*670-18del	ENSP00000503979.1:n.*670-18del
ENST00000677625.1:c.1196-18del	ENSP00000502857.1:n.1196-18del
ENST00000677856.1:n.1503-18del
ENST00000677915.1:c.*147-18del	ENSP00000503118.1:n.*147-18del
ENST00000678533.1:c.*804-18del	ENSP00000503873.1:n.*804-18del
ENST00000678592.1:c.*190-18del	ENSP00000504424.1:n.*190-18del
ENST00000278407.8:c.1250-18del	ENSP00000278407.4:n.1250-18del
ENST00000340687.10:c.1139-18del	ENSP00000341861.6:n.1139-18del
ENST00000378323.8:c.1265-18del	ENSP00000367574.4:n.1265-18del
ENST00000378324.6:c.1094-18del	ENSP00000367575.2:n.1094-18del
ENST00000403558.1:c.1379-18del	ENSP00000384420.1:n.1379-18del
ENST00000528996.1:c.451-18del	ENSP00000431226.1:n.451-18del
ENST00000530113.1:n.707-18del
ENST00000531133.5:c.751-18del	ENSP00000435431.1:n.751-18del
ENST00000531797.5:c.*275-18del	ENSP00000432554.1:n.*275-18del
ENST00000619430.1:c.381-18del	ENSP00000478572.1:n.381-18del
NM_000062.2:c.1250-18del , LRG_105t1:c.1250-18del	NP_000053.2:n.1250-18del
NM_001032295.1:c.1250-18del	NP_001027466.1:n.1250-18del
NM_000062.3:c.1250-18del MANE Select	NP_000053.2:n.1250-18del
NM_001032295.2:c.1250-18del	NP_001027466.1:n.1250-18del