Canonical Allele Identifier: CA380690765

Gene: SERPING1

Linked Data

• dbSNP Id: rs1945516304
• MyVariant Identifiers: chr11:g.57381962T>G (hg19) ; chr11:g.57614489T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614489T>G , CM000673.2:g.57614489T>G	GRCh38
NC_000011.9:g.57381962T>G , CM000673.1:g.57381962T>G	GRCh37
NC_000011.8:g.57138538T>G	NCBI36
NG_009625.1:g.21936T>G , LRG_105:g.21936T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1411T>G MANE Select	ENSP00000278407.4:p.Phe471Val
ENST00000528996.2:c.*308T>G	ENSP00000431226.2:n.*308T>G
ENST00000531605.2:c.*1187T>G	ENSP00000503752.1:n.*1187T>G
ENST00000619430.2:c.1207T>G	ENSP00000478572.2:p.Phe403Val
ENST00000676670.1:c.1411T>G	ENSP00000504807.1:p.Phe471Val
ENST00000676741.1:n.2493T>G
ENST00000677624.1:c.*831T>G	ENSP00000503979.1:n.*831T>G
ENST00000677625.1:c.1357T>G	ENSP00000502857.1:p.Phe453Val
ENST00000677856.1:n.1664T>G
ENST00000677915.1:c.*308T>G	ENSP00000503118.1:n.*308T>G
ENST00000678533.1:c.*965T>G	ENSP00000503873.1:n.*965T>G
ENST00000678592.1:c.*351T>G	ENSP00000504424.1:n.*351T>G
ENST00000278407.8:c.1411T>G	ENSP00000278407.4:p.Phe471Val
ENST00000340687.10:c.1300T>G	ENSP00000341861.6:p.Phe434Val
ENST00000378323.8:c.1426T>G	ENSP00000367574.4:p.Phe476Val
ENST00000378324.6:c.1255T>G	ENSP00000367575.2:p.Phe419Val
ENST00000403558.1:c.1540T>G	ENSP00000384420.1:p.Phe514Val
ENST00000528996.1:c.612T>G	ENSP00000431226.1:n.612T>G
ENST00000530113.1:n.868T>G
ENST00000531133.5:c.912T>G	ENSP00000435431.1:n.912T>G
ENST00000531797.5:c.*436T>G	ENSP00000432554.1:n.*436T>G
ENST00000619430.1:c.542T>G	ENSP00000478572.1:n.542T>G
NM_000062.2:c.1411T>G , LRG_105t1:c.1411T>G	NP_000053.2:p.Phe471Val
NM_001032295.1:c.1411T>G	NP_001027466.1:p.Phe471Val
NM_000062.3:c.1411T>G MANE Select	NP_000053.2:p.Phe471Val
NM_001032295.2:c.1411T>G	NP_001027466.1:p.Phe471Val