Canonical Allele Identifier: CA380702429

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57379218T>A (hg19) ; chr11:g.57611745T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611745T>A , CM000673.2:g.57611745T>A	GRCh38
NC_000011.9:g.57379218T>A , CM000673.1:g.57379218T>A	GRCh37
NC_000011.8:g.57135794T>A	NCBI36
NG_009625.1:g.19192T>A , LRG_105:g.19192T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1058T>A MANE Select	ENSP00000278407.4:p.Leu353Gln
ENST00000528996.2:c.78T>A	ENSP00000431226.2:p.Ser26=
ENST00000531605.2:c.*834T>A	ENSP00000503752.1:n.*834T>A
ENST00000619430.2:c.854T>A	ENSP00000478572.2:p.Leu285Gln
ENST00000676670.1:c.1058T>A	ENSP00000504807.1:p.Leu353Gln
ENST00000676741.1:n.2140T>A
ENST00000677624.1:c.*478T>A	ENSP00000503979.1:n.*478T>A
ENST00000677625.1:c.1030-26T>A	ENSP00000502857.1:n.1030-26T>A
ENST00000677856.1:n.1311T>A
ENST00000677915.1:c.714T>A	ENSP00000503118.1:p.Ser238=
ENST00000678533.1:c.*612T>A	ENSP00000503873.1:n.*612T>A
ENST00000678592.1:c.1147T>A	ENSP00000504424.1:p.Ter383Arg
ENST00000278407.8:c.1058T>A	ENSP00000278407.4:p.Leu353Gln
ENST00000340687.10:c.1030-83T>A	ENSP00000341861.6:n.1030-83T>A
ENST00000378323.8:c.1073T>A	ENSP00000367574.4:p.Leu358Gln
ENST00000378324.6:c.902T>A	ENSP00000367575.2:p.Leu301Gln
ENST00000403558.1:c.1187T>A	ENSP00000384420.1:p.Leu396Gln
ENST00000528996.1:c.259T>A	ENSP00000431226.1:p.Ter87Arg
ENST00000530113.1:n.515T>A
ENST00000531133.5:c.559T>A	ENSP00000435431.1:n.559T>A
ENST00000531797.5:c.*83T>A	ENSP00000432554.1:n.*83T>A
ENST00000619430.1:c.349-160T>A	ENSP00000478572.1:n.349-160T>A
NM_000062.2:c.1058T>A , LRG_105t1:c.1058T>A	NP_000053.2:p.Leu353Gln
NM_001032295.1:c.1058T>A	NP_001027466.1:p.Leu353Gln
NM_000062.3:c.1058T>A MANE Select	NP_000053.2:p.Leu353Gln
NM_001032295.2:c.1058T>A	NP_001027466.1:p.Leu353Gln