Canonical Allele Identifier: CA10603251
Gene: SERPING1 HGNC NCBI

Linked Data

ClinVar Variation Id: 280064
ClinVar RCV Id: RCV000329390
dbSNP Id: rs886041353
MyVariant Identifiers: chr11:g.57367351G>A (hg19) chr11:g.57599878G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57599878G>A , CM000673.2:g.57599878G>A GRCh38
NC_000011.9:g.57367351G>A , CM000673.1:g.57367351G>A GRCh37
NC_000011.8:g.57123927G>A NCBI36
NG_009625.1:g.7325G>A , LRG_105:g.7325G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000278407.9:c.52-1G>A MANE Select ENSP00000278407.4:n.52-1G>A
ENST00000528996.2:c.58+1550G>A ENSP00000431226.2:n.58+1550G>A
ENST00000531605.2:c.51+1557G>A ENSP00000503752.1:n.51+1557G>A
ENST00000619430.2:c.52-1G>A ENSP00000478572.2:n.52-1G>A
ENST00000676670.1:c.52-1G>A ENSP00000504807.1:n.52-1G>A
ENST00000676741.1:n.1133G>A
ENST00000677275.1:n.39-1G>A
ENST00000677624.1:c.52-1G>A ENSP00000503979.1:n.52-1G>A
ENST00000677625.1:c.52-1G>A ENSP00000502857.1:n.52-1G>A
ENST00000677856.1:n.111-1G>A
ENST00000677915.1:c.52-1G>A ENSP00000503118.1:n.52-1G>A
ENST00000678533.1:c.51+1557G>A ENSP00000503873.1:n.51+1557G>A
ENST00000678592.1:c.52-1G>A ENSP00000504424.1:n.52-1G>A
ENST00000278407.8:c.52-1G>A ENSP00000278407.4:n.52-1G>A
ENST00000340687.10:c.52-1G>A ENSP00000341861.6:n.52-1G>A
ENST00000378323.8:c.66G>A ENSP00000367574.4:p.Gln22=
ENST00000378324.6:c.-105-1G>A ENSP00000367575.2:n.-105-1G>A
ENST00000403558.1:c.154-1G>A ENSP00000384420.1:n.154-1G>A
ENST00000405496.5:c.52-1G>A ENSP00000384561.1:n.52-1G>A
ENST00000457869.1:c.154-1G>A ENSP00000399746.1:n.154-1G>A
ENST00000531133.5:c.51+1557G>A ENSP00000435431.1:n.51+1557G>A
ENST00000531797.5:c.51+1557G>A ENSP00000432554.1:n.51+1557G>A
ENST00000619430.1:c.52-1G>A ENSP00000478572.1:n.52-1G>A
NM_000062.2:c.52-1G>A , LRG_105t1:c.52-1G>A NP_000053.2:n.52-1G>A
NM_001032295.1:c.52-1G>A NP_001027466.1:n.52-1G>A
NM_000062.3:c.52-1G>A MANE Select NP_000053.2:n.52-1G>A
NM_001032295.2:c.52-1G>A NP_001027466.1:n.52-1G>A
Search 100 bp 5'
Search 100 bp 3'