Canonical Allele Identifier: CA380703174

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57379332T>A (hg19) ; chr11:g.57611859T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611859T>A , CM000673.2:g.57611859T>A	GRCh38
NC_000011.9:g.57379332T>A , CM000673.1:g.57379332T>A	GRCh37
NC_000011.8:g.57135908T>A	NCBI36
NG_009625.1:g.19306T>A , LRG_105:g.19306T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.1172T>A MANE Select	ENSP00000278407.4:p.Phe391Tyr
ENST00000528996.2:c.*69T>A	ENSP00000431226.2:n.*69T>A
ENST00000531605.2:c.*948T>A	ENSP00000503752.1:n.*948T>A
ENST00000619430.2:c.968T>A	ENSP00000478572.2:p.Phe323Tyr
ENST00000676670.1:c.1172T>A	ENSP00000504807.1:p.Phe391Tyr
ENST00000676741.1:n.2254T>A
ENST00000677624.1:c.*592T>A	ENSP00000503979.1:n.*592T>A
ENST00000677625.1:c.1118T>A	ENSP00000502857.1:p.Phe373Tyr
ENST00000677856.1:n.1425T>A
ENST00000677915.1:c.*69T>A	ENSP00000503118.1:n.*69T>A
ENST00000678533.1:c.*726T>A	ENSP00000503873.1:n.*726T>A
ENST00000678592.1:c.*112T>A	ENSP00000504424.1:n.*112T>A
ENST00000278407.8:c.1172T>A	ENSP00000278407.4:p.Phe391Tyr
ENST00000340687.10:c.1061T>A	ENSP00000341861.6:p.Phe354Tyr
ENST00000378323.8:c.1187T>A	ENSP00000367574.4:p.Phe396Tyr
ENST00000378324.6:c.1016T>A	ENSP00000367575.2:p.Phe339Tyr
ENST00000403558.1:c.1301T>A	ENSP00000384420.1:p.Phe434Tyr
ENST00000528996.1:c.373T>A	ENSP00000431226.1:n.373T>A
ENST00000530113.1:n.629T>A
ENST00000531133.5:c.673T>A	ENSP00000435431.1:n.673T>A
ENST00000531797.5:c.*197T>A	ENSP00000432554.1:n.*197T>A
ENST00000619430.1:c.349-46T>A	ENSP00000478572.1:n.349-46T>A
NM_000062.2:c.1172T>A , LRG_105t1:c.1172T>A	NP_000053.2:p.Phe391Tyr
NM_001032295.1:c.1172T>A	NP_001027466.1:p.Phe391Tyr
NM_000062.3:c.1172T>A MANE Select	NP_000053.2:p.Phe391Tyr
NM_001032295.2:c.1172T>A	NP_001027466.1:p.Phe391Tyr