Canonical Allele Identifier: CA380690857

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57382001C>A (hg19) ; chr11:g.57614528C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614528C>A , CM000673.2:g.57614528C>A	GRCh38
NC_000011.9:g.57382001C>A , CM000673.1:g.57382001C>A	GRCh37
NC_000011.8:g.57138577C>A	NCBI36
NG_009625.1:g.21975C>A , LRG_105:g.21975C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1450C>A MANE Select	ENSP00000278407.4:p.Gln484Lys
ENST00000528996.2:c.*347C>A	ENSP00000431226.2:n.*347C>A
ENST00000531605.2:c.*1226C>A	ENSP00000503752.1:n.*1226C>A
ENST00000619430.2:c.1246C>A	ENSP00000478572.2:p.Gln416Lys
ENST00000676670.1:c.1450C>A	ENSP00000504807.1:p.Gln484Lys
ENST00000676741.1:n.2532C>A
ENST00000677624.1:c.*870C>A	ENSP00000503979.1:n.*870C>A
ENST00000677625.1:c.1396C>A	ENSP00000502857.1:p.Gln466Lys
ENST00000677856.1:n.1703C>A
ENST00000677915.1:c.*347C>A	ENSP00000503118.1:n.*347C>A
ENST00000678533.1:c.*1004C>A	ENSP00000503873.1:n.*1004C>A
ENST00000678592.1:c.*390C>A	ENSP00000504424.1:n.*390C>A
ENST00000278407.8:c.1450C>A	ENSP00000278407.4:p.Gln484Lys
ENST00000340687.10:c.1339C>A	ENSP00000341861.6:p.Gln447Lys
ENST00000378323.8:c.1465C>A	ENSP00000367574.4:p.Gln489Lys
ENST00000378324.6:c.1294C>A	ENSP00000367575.2:p.Gln432Lys
ENST00000403558.1:c.1579C>A	ENSP00000384420.1:p.Gln527Lys
ENST00000528996.1:c.651C>A	ENSP00000431226.1:n.651C>A
ENST00000530113.1:n.907C>A
ENST00000531133.5:c.951C>A	ENSP00000435431.1:n.951C>A
ENST00000531797.5:c.*475C>A	ENSP00000432554.1:n.*475C>A
ENST00000619430.1:c.581C>A	ENSP00000478572.1:n.581C>A
NM_000062.2:c.1450C>A , LRG_105t1:c.1450C>A	NP_000053.2:p.Gln484Lys
NM_001032295.1:c.1450C>A	NP_001027466.1:p.Gln484Lys
NM_000062.3:c.1450C>A MANE Select	NP_000053.2:p.Gln484Lys
NM_001032295.2:c.1450C>A	NP_001027466.1:p.Gln484Lys