Canonical Allele Identifier: CA380690761

Gene: SERPING1

Linked Data

• ClinVar Variation Id: 877134
• ClinVar RCV Id: RCV001102619
• dbSNP Id: rs1590831488
• MyVariant Identifiers: chr11:g.57381960T>A (hg19) ; chr11:g.57614487T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614487T>A , CM000673.2:g.57614487T>A	GRCh38
NC_000011.9:g.57381960T>A , CM000673.1:g.57381960T>A	GRCh37
NC_000011.8:g.57138536T>A	NCBI36
NG_009625.1:g.21934T>A , LRG_105:g.21934T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1409T>A MANE Select	ENSP00000278407.4:p.Val470Asp
ENST00000528996.2:c.*306T>A	ENSP00000431226.2:n.*306T>A
ENST00000531605.2:c.*1185T>A	ENSP00000503752.1:n.*1185T>A
ENST00000619430.2:c.1205T>A	ENSP00000478572.2:p.Val402Asp
ENST00000676670.1:c.1409T>A	ENSP00000504807.1:p.Val470Asp
ENST00000676741.1:n.2491T>A
ENST00000677624.1:c.*829T>A	ENSP00000503979.1:n.*829T>A
ENST00000677625.1:c.1355T>A	ENSP00000502857.1:p.Val452Asp
ENST00000677856.1:n.1662T>A
ENST00000677915.1:c.*306T>A	ENSP00000503118.1:n.*306T>A
ENST00000678533.1:c.*963T>A	ENSP00000503873.1:n.*963T>A
ENST00000678592.1:c.*349T>A	ENSP00000504424.1:n.*349T>A
ENST00000278407.8:c.1409T>A	ENSP00000278407.4:p.Val470Asp
ENST00000340687.10:c.1298T>A	ENSP00000341861.6:p.Val433Asp
ENST00000378323.8:c.1424T>A	ENSP00000367574.4:p.Val475Asp
ENST00000378324.6:c.1253T>A	ENSP00000367575.2:p.Val418Asp
ENST00000403558.1:c.1538T>A	ENSP00000384420.1:p.Val513Asp
ENST00000528996.1:c.610T>A	ENSP00000431226.1:n.610T>A
ENST00000530113.1:n.866T>A
ENST00000531133.5:c.910T>A	ENSP00000435431.1:n.910T>A
ENST00000531797.5:c.*434T>A	ENSP00000432554.1:n.*434T>A
ENST00000619430.1:c.540T>A	ENSP00000478572.1:n.540T>A
NM_000062.2:c.1409T>A , LRG_105t1:c.1409T>A	NP_000053.2:p.Val470Asp
NM_001032295.1:c.1409T>A	NP_001027466.1:p.Val470Asp
NM_000062.3:c.1409T>A MANE Select	NP_000053.2:p.Val470Asp
NM_001032295.2:c.1409T>A	NP_001027466.1:p.Val470Asp