Canonical Allele Identifier: CA380703517

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57379399G>A (hg19) ; chr11:g.57611926G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611926G>A , CM000673.2:g.57611926G>A	GRCh38
NC_000011.9:g.57379399G>A , CM000673.1:g.57379399G>A	GRCh37
NC_000011.8:g.57135975G>A	NCBI36
NG_009625.1:g.19373G>A , LRG_105:g.19373G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1239G>A MANE Select	ENSP00000278407.4:p.Met413Ile
ENST00000528996.2:c.*136G>A	ENSP00000431226.2:n.*136G>A
ENST00000531605.2:c.*1015G>A	ENSP00000503752.1:n.*1015G>A
ENST00000619430.2:c.1035G>A	ENSP00000478572.2:p.Met345Ile
ENST00000676670.1:c.1239G>A	ENSP00000504807.1:p.Met413Ile
ENST00000676741.1:n.2321G>A
ENST00000677624.1:c.*659G>A	ENSP00000503979.1:n.*659G>A
ENST00000677625.1:c.1185G>A	ENSP00000502857.1:p.Met395Ile
ENST00000677856.1:n.1492G>A
ENST00000677915.1:c.*136G>A	ENSP00000503118.1:n.*136G>A
ENST00000678533.1:c.*793G>A	ENSP00000503873.1:n.*793G>A
ENST00000678592.1:c.*179G>A	ENSP00000504424.1:n.*179G>A
ENST00000278407.8:c.1239G>A	ENSP00000278407.4:p.Met413Ile
ENST00000340687.10:c.1128G>A	ENSP00000341861.6:p.Met376Ile
ENST00000378323.8:c.1254G>A	ENSP00000367574.4:p.Met418Ile
ENST00000378324.6:c.1083G>A	ENSP00000367575.2:p.Met361Ile
ENST00000403558.1:c.1368G>A	ENSP00000384420.1:p.Met456Ile
ENST00000528996.1:c.440G>A	ENSP00000431226.1:n.440G>A
ENST00000530113.1:n.696G>A
ENST00000531133.5:c.740G>A	ENSP00000435431.1:n.740G>A
ENST00000531797.5:c.*264G>A	ENSP00000432554.1:n.*264G>A
ENST00000619430.1:c.370G>A	ENSP00000478572.1:p.Gly124Arg
NM_000062.2:c.1239G>A , LRG_105t1:c.1239G>A	NP_000053.2:p.Met413Ile
NM_001032295.1:c.1239G>A	NP_001027466.1:p.Met413Ile
NM_000062.3:c.1239G>A MANE Select	NP_000053.2:p.Met413Ile
NM_001032295.2:c.1239G>A	NP_001027466.1:p.Met413Ile