Canonical Allele Identifier: CA223024142

Gene: SERPING1

Linked Data

• dbSNP Id: rs770530066
• gnomAD v4: 11-57614279-A-T
• MyVariant Identifiers: chr11:g.57381752A>T (hg19) ; chr11:g.57614279A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614279A>T , CM000673.2:g.57614279A>T	GRCh38
NC_000011.9:g.57381752A>T , CM000673.1:g.57381752A>T	GRCh37
NC_000011.8:g.57138328A>T	NCBI36
NG_009625.1:g.21726A>T , LRG_105:g.21726A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1250-49A>T MANE Select	ENSP00000278407.4:n.1250-49A>T
ENST00000528996.2:c.*147-49A>T	ENSP00000431226.2:n.*147-49A>T
ENST00000531605.2:c.*1026-49A>T	ENSP00000503752.1:n.*1026-49A>T
ENST00000619430.2:c.1046-49A>T	ENSP00000478572.2:n.1046-49A>T
ENST00000676670.1:c.1250-49A>T	ENSP00000504807.1:n.1250-49A>T
ENST00000676741.1:n.2332-49A>T
ENST00000677624.1:c.*670-49A>T	ENSP00000503979.1:n.*670-49A>T
ENST00000677625.1:c.1196-49A>T	ENSP00000502857.1:n.1196-49A>T
ENST00000677856.1:n.1503-49A>T
ENST00000677915.1:c.*147-49A>T	ENSP00000503118.1:n.*147-49A>T
ENST00000678533.1:c.*804-49A>T	ENSP00000503873.1:n.*804-49A>T
ENST00000678592.1:c.*190-49A>T	ENSP00000504424.1:n.*190-49A>T
ENST00000278407.8:c.1250-49A>T	ENSP00000278407.4:n.1250-49A>T
ENST00000340687.10:c.1139-49A>T	ENSP00000341861.6:n.1139-49A>T
ENST00000378323.8:c.1265-49A>T	ENSP00000367574.4:n.1265-49A>T
ENST00000378324.6:c.1094-49A>T	ENSP00000367575.2:n.1094-49A>T
ENST00000403558.1:c.1379-49A>T	ENSP00000384420.1:n.1379-49A>T
ENST00000528996.1:c.451-49A>T	ENSP00000431226.1:n.451-49A>T
ENST00000530113.1:n.707-49A>T
ENST00000531133.5:c.751-49A>T	ENSP00000435431.1:n.751-49A>T
ENST00000531797.5:c.*275-49A>T	ENSP00000432554.1:n.*275-49A>T
ENST00000619430.1:c.381-49A>T	ENSP00000478572.1:n.381-49A>T
NM_000062.2:c.1250-49A>T , LRG_105t1:c.1250-49A>T	NP_000053.2:n.1250-49A>T
NM_001032295.1:c.1250-49A>T	NP_001027466.1:n.1250-49A>T
NM_000062.3:c.1250-49A>T MANE Select	NP_000053.2:n.1250-49A>T
NM_001032295.2:c.1250-49A>T	NP_001027466.1:n.1250-49A>T