Canonical Allele Identifier: CA380702563

Gene: SERPING1

Linked Data

• ClinVar Variation Id: 2443257
• ClinVar RCV Id: RCV003151649
• MyVariant Identifiers: chr11:g.57379241C>T (hg19) ; chr11:g.57611768C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611768C>T , CM000673.2:g.57611768C>T	GRCh38
NC_000011.9:g.57379241C>T , CM000673.1:g.57379241C>T	GRCh37
NC_000011.8:g.57135817C>T	NCBI36
NG_009625.1:g.19215C>T , LRG_105:g.19215C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.1081C>T MANE Select	ENSP00000278407.4:p.Gln361Ter
ENST00000528996.2:c.101C>T	ENSP00000431226.2:p.Pro34Leu
ENST00000531605.2:c.*857C>T	ENSP00000503752.1:n.*857C>T
ENST00000619430.2:c.877C>T	ENSP00000478572.2:p.Gln293Ter
ENST00000676670.1:c.1081C>T	ENSP00000504807.1:p.Gln361Ter
ENST00000676741.1:n.2163C>T
ENST00000677624.1:c.*501C>T	ENSP00000503979.1:n.*501C>T
ENST00000677625.1:c.1030-3C>T	ENSP00000502857.1:n.1030-3C>T
ENST00000677856.1:n.1334C>T
ENST00000677915.1:c.737C>T	ENSP00000503118.1:p.Pro246Leu
ENST00000678533.1:c.*635C>T	ENSP00000503873.1:n.*635C>T
ENST00000678592.1:c.*21C>T	ENSP00000504424.1:n.*21C>T
ENST00000278407.8:c.1081C>T	ENSP00000278407.4:p.Gln361Ter
ENST00000340687.10:c.1030-60C>T	ENSP00000341861.6:n.1030-60C>T
ENST00000378323.8:c.1096C>T	ENSP00000367574.4:p.Gln366Ter
ENST00000378324.6:c.925C>T	ENSP00000367575.2:p.Gln309Ter
ENST00000403558.1:c.1210C>T	ENSP00000384420.1:p.Gln404Ter
ENST00000528996.1:c.282C>T	ENSP00000431226.1:n.282C>T
ENST00000530113.1:n.538C>T
ENST00000531133.5:c.582C>T	ENSP00000435431.1:n.582C>T
ENST00000531797.5:c.*106C>T	ENSP00000432554.1:n.*106C>T
ENST00000619430.1:c.349-137C>T	ENSP00000478572.1:n.349-137C>T
NM_000062.2:c.1081C>T , LRG_105t1:c.1081C>T	NP_000053.2:p.Gln361Ter
NM_001032295.1:c.1081C>T	NP_001027466.1:p.Gln361Ter
NM_000062.3:c.1081C>T MANE Select	NP_000053.2:p.Gln361Ter
NM_001032295.2:c.1081C>T	NP_001027466.1:p.Gln361Ter