Canonical Allele Identifier: CA6008014

Gene: SERPING1

Linked Data

• ClinVar Variation Id: 1206197
• ClinVar RCV Id: RCV001573519
• dbSNP Id: rs750408264
• ExAC: 11:57367583 A / C
• gnomAD v2: 11-57367583-A-C
• gnomAD v3: 11-57600110-A-C
• gnomAD v4: 11-57600110-A-C
• MyVariant Identifiers: chr11:g.57367583A>C (hg19) ; chr11:g.57600110A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57600110A>C , CM000673.2:g.57600110A>C	GRCh38
NC_000011.9:g.57367583A>C , CM000673.1:g.57367583A>C	GRCh37
NC_000011.8:g.57124159A>C	NCBI36
NG_009625.1:g.7557A>C , LRG_105:g.7557A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.283A>C MANE Select	ENSP00000278407.4:p.Thr95Pro
ENST00000528996.2:c.58+1782A>C	ENSP00000431226.2:n.58+1782A>C
ENST00000531605.2:c.51+1789A>C	ENSP00000503752.1:n.51+1789A>C
ENST00000619430.2:c.283A>C	ENSP00000478572.2:p.Thr95Pro
ENST00000676670.1:c.283A>C	ENSP00000504807.1:p.Thr95Pro
ENST00000676741.1:n.1365A>C
ENST00000677275.1:n.270A>C
ENST00000677624.1:c.283A>C	ENSP00000503979.1:p.Thr95Pro
ENST00000677625.1:c.283A>C	ENSP00000502857.1:p.Thr95Pro
ENST00000677856.1:n.342A>C
ENST00000677915.1:c.283A>C	ENSP00000503118.1:p.Thr95Pro
ENST00000678533.1:c.51+1789A>C	ENSP00000503873.1:n.51+1789A>C
ENST00000678592.1:c.283A>C	ENSP00000504424.1:p.Thr95Pro
ENST00000278407.8:c.283A>C	ENSP00000278407.4:p.Thr95Pro
ENST00000340687.10:c.283A>C	ENSP00000341861.6:p.Thr95Pro
ENST00000378323.8:c.298A>C	ENSP00000367574.4:p.Thr100Pro
ENST00000378324.6:c.127A>C	ENSP00000367575.2:p.Thr43Pro
ENST00000403558.1:c.385A>C	ENSP00000384420.1:p.Thr129Pro
ENST00000405496.5:c.283A>C	ENSP00000384561.1:p.Thr95Pro
ENST00000531133.5:c.51+1789A>C	ENSP00000435431.1:n.51+1789A>C
ENST00000531797.5:c.51+1789A>C	ENSP00000432554.1:n.51+1789A>C
ENST00000619430.1:c.283A>C	ENSP00000478572.1:p.Thr95Pro
NM_000062.2:c.283A>C , LRG_105t1:c.283A>C	NP_000053.2:p.Thr95Pro
NM_001032295.1:c.283A>C	NP_001027466.1:p.Thr95Pro
NM_000062.3:c.283A>C MANE Select	NP_000053.2:p.Thr95Pro
NM_001032295.2:c.283A>C	NP_001027466.1:p.Thr95Pro