Canonical Allele Identifier: CA380690216

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381817T>A (hg19) ; chr11:g.57614344T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614344T>A , CM000673.2:g.57614344T>A	GRCh38
NC_000011.9:g.57381817T>A , CM000673.1:g.57381817T>A	GRCh37
NC_000011.8:g.57138393T>A	NCBI36
NG_009625.1:g.21791T>A , LRG_105:g.21791T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1266T>A MANE Select	ENSP00000278407.4:p.Ser422=
ENST00000528996.2:c.*163T>A	ENSP00000431226.2:n.*163T>A
ENST00000531605.2:c.*1042T>A	ENSP00000503752.1:n.*1042T>A
ENST00000619430.2:c.1062T>A	ENSP00000478572.2:p.Ser354=
ENST00000676670.1:c.1266T>A	ENSP00000504807.1:p.Ser422=
ENST00000676741.1:n.2348T>A
ENST00000677624.1:c.*686T>A	ENSP00000503979.1:n.*686T>A
ENST00000677625.1:c.1212T>A	ENSP00000502857.1:p.Ser404=
ENST00000677856.1:n.1519T>A
ENST00000677915.1:c.*163T>A	ENSP00000503118.1:n.*163T>A
ENST00000678533.1:c.*820T>A	ENSP00000503873.1:n.*820T>A
ENST00000678592.1:c.*206T>A	ENSP00000504424.1:n.*206T>A
ENST00000278407.8:c.1266T>A	ENSP00000278407.4:p.Ser422=
ENST00000340687.10:c.1155T>A	ENSP00000341861.6:p.Ser385=
ENST00000378323.8:c.1281T>A	ENSP00000367574.4:p.Ser427=
ENST00000378324.6:c.1110T>A	ENSP00000367575.2:p.Ser370=
ENST00000403558.1:c.1395T>A	ENSP00000384420.1:p.Ser465=
ENST00000528996.1:c.467T>A	ENSP00000431226.1:n.467T>A
ENST00000530113.1:n.723T>A
ENST00000531133.5:c.767T>A	ENSP00000435431.1:n.767T>A
ENST00000531797.5:c.*291T>A	ENSP00000432554.1:n.*291T>A
ENST00000619430.1:c.397T>A	ENSP00000478572.1:p.Leu133Ile
NM_000062.2:c.1266T>A , LRG_105t1:c.1266T>A	NP_000053.2:p.Ser422=
NM_001032295.1:c.1266T>A	NP_001027466.1:p.Ser422=
NM_000062.3:c.1266T>A MANE Select	NP_000053.2:p.Ser422=
NM_001032295.2:c.1266T>A	NP_001027466.1:p.Ser422=