Canonical Allele Identifier: CA380703169

Gene: SERPING1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.1172T>C MANE Select	ENSP00000278407.4:p.Phe391Ser
ENST00000528996.2:c.*69T>C	ENSP00000431226.2:n.*69T>C
ENST00000531605.2:c.*948T>C	ENSP00000503752.1:n.*948T>C
ENST00000619430.2:c.968T>C	ENSP00000478572.2:p.Phe323Ser
ENST00000676670.1:c.1172T>C	ENSP00000504807.1:p.Phe391Ser
ENST00000676741.1:n.2254T>C
ENST00000677624.1:c.*592T>C	ENSP00000503979.1:n.*592T>C
ENST00000677625.1:c.1118T>C	ENSP00000502857.1:p.Phe373Ser
ENST00000677856.1:n.1425T>C
ENST00000677915.1:c.*69T>C	ENSP00000503118.1:n.*69T>C
ENST00000678533.1:c.*726T>C	ENSP00000503873.1:n.*726T>C
ENST00000678592.1:c.*112T>C	ENSP00000504424.1:n.*112T>C
ENST00000278407.8:c.1172T>C	ENSP00000278407.4:p.Phe391Ser
ENST00000340687.10:c.1061T>C	ENSP00000341861.6:p.Phe354Ser
ENST00000378323.8:c.1187T>C	ENSP00000367574.4:p.Phe396Ser
ENST00000378324.6:c.1016T>C	ENSP00000367575.2:p.Phe339Ser
ENST00000403558.1:c.1301T>C	ENSP00000384420.1:p.Phe434Ser
ENST00000528996.1:c.373T>C	ENSP00000431226.1:n.373T>C
ENST00000530113.1:n.629T>C
ENST00000531133.5:c.673T>C	ENSP00000435431.1:n.673T>C
ENST00000531797.5:c.*197T>C	ENSP00000432554.1:n.*197T>C
ENST00000619430.1:c.349-46T>C	ENSP00000478572.1:n.349-46T>C
NM_000062.2:c.1172T>C , LRG_105t1:c.1172T>C	NP_000053.2:p.Phe391Ser
NM_001032295.1:c.1172T>C	NP_001027466.1:p.Phe391Ser
NM_000062.3:c.1172T>C MANE Select	NP_000053.2:p.Phe391Ser
NM_001032295.2:c.1172T>C	NP_001027466.1:p.Phe391Ser