Canonical Allele Identifier: CA380690845

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381996G>T (hg19) ; chr11:g.57614523G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614523G>T , CM000673.2:g.57614523G>T	GRCh38
NC_000011.9:g.57381996G>T , CM000673.1:g.57381996G>T	GRCh37
NC_000011.8:g.57138572G>T	NCBI36
NG_009625.1:g.21970G>T , LRG_105:g.21970G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1445G>T MANE Select	ENSP00000278407.4:p.Trp482Leu
ENST00000528996.2:c.*342G>T	ENSP00000431226.2:n.*342G>T
ENST00000531605.2:c.*1221G>T	ENSP00000503752.1:n.*1221G>T
ENST00000619430.2:c.1241G>T	ENSP00000478572.2:p.Trp414Leu
ENST00000676670.1:c.1445G>T	ENSP00000504807.1:p.Trp482Leu
ENST00000676741.1:n.2527G>T
ENST00000677624.1:c.*865G>T	ENSP00000503979.1:n.*865G>T
ENST00000677625.1:c.1391G>T	ENSP00000502857.1:p.Trp464Leu
ENST00000677856.1:n.1698G>T
ENST00000677915.1:c.*342G>T	ENSP00000503118.1:n.*342G>T
ENST00000678533.1:c.*999G>T	ENSP00000503873.1:n.*999G>T
ENST00000678592.1:c.*385G>T	ENSP00000504424.1:n.*385G>T
ENST00000278407.8:c.1445G>T	ENSP00000278407.4:p.Trp482Leu
ENST00000340687.10:c.1334G>T	ENSP00000341861.6:p.Trp445Leu
ENST00000378323.8:c.1460G>T	ENSP00000367574.4:p.Trp487Leu
ENST00000378324.6:c.1289G>T	ENSP00000367575.2:p.Trp430Leu
ENST00000403558.1:c.1574G>T	ENSP00000384420.1:p.Trp525Leu
ENST00000528996.1:c.646G>T	ENSP00000431226.1:n.646G>T
ENST00000530113.1:n.902G>T
ENST00000531133.5:c.946G>T	ENSP00000435431.1:n.946G>T
ENST00000531797.5:c.*470G>T	ENSP00000432554.1:n.*470G>T
ENST00000619430.1:c.576G>T	ENSP00000478572.1:n.576G>T
NM_000062.2:c.1445G>T , LRG_105t1:c.1445G>T	NP_000053.2:p.Trp482Leu
NM_001032295.1:c.1445G>T	NP_001027466.1:p.Trp482Leu
NM_000062.3:c.1445G>T MANE Select	NP_000053.2:p.Trp482Leu
NM_001032295.2:c.1445G>T	NP_001027466.1:p.Trp482Leu