Canonical Allele Identifier: CA474806878

Gene: SERPING1

Linked Data

• gnomAD v4: 11-57614479-C-A
• MyVariant Identifiers: chr11:g.57381952C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614479C>A , CM000673.2:g.57614479C>A	GRCh38
NC_000011.9:g.57381952C>A , CM000673.1:g.57381952C>A	GRCh37
NC_000011.8:g.57138528C>A	NCBI36
NG_009625.1:g.21926C>A , LRG_105:g.21926C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1401C>A MANE Select	ENSP00000278407.4:p.Thr467=
ENST00000528996.2:c.*298C>A	ENSP00000431226.2:n.*298C>A
ENST00000531605.2:c.*1177C>A	ENSP00000503752.1:n.*1177C>A
ENST00000619430.2:c.1197C>A	ENSP00000478572.2:p.Thr399=
ENST00000676670.1:c.1401C>A	ENSP00000504807.1:p.Thr467=
ENST00000676741.1:n.2483C>A
ENST00000677624.1:c.*821C>A	ENSP00000503979.1:n.*821C>A
ENST00000677625.1:c.1347C>A	ENSP00000502857.1:p.Thr449=
ENST00000677856.1:n.1654C>A
ENST00000677915.1:c.*298C>A	ENSP00000503118.1:n.*298C>A
ENST00000678533.1:c.*955C>A	ENSP00000503873.1:n.*955C>A
ENST00000678592.1:c.*341C>A	ENSP00000504424.1:n.*341C>A
ENST00000278407.8:c.1401C>A	ENSP00000278407.4:p.Thr467=
ENST00000340687.10:c.1290C>A	ENSP00000341861.6:p.Thr430=
ENST00000378323.8:c.1416C>A	ENSP00000367574.4:p.Thr472=
ENST00000378324.6:c.1245C>A	ENSP00000367575.2:p.Thr415=
ENST00000403558.1:c.1530C>A	ENSP00000384420.1:p.Thr510=
ENST00000528996.1:c.602C>A	ENSP00000431226.1:n.602C>A
ENST00000530113.1:n.858C>A
ENST00000531133.5:c.902C>A	ENSP00000435431.1:n.902C>A
ENST00000531797.5:c.*426C>A	ENSP00000432554.1:n.*426C>A
ENST00000619430.1:c.532C>A	ENSP00000478572.1:n.532C>A
NM_000062.2:c.1401C>A , LRG_105t1:c.1401C>A	NP_000053.2:p.Thr467=
NM_001032295.1:c.1401C>A	NP_001027466.1:p.Thr467=
NM_000062.3:c.1401C>A MANE Select	NP_000053.2:p.Thr467=
NM_001032295.2:c.1401C>A	NP_001027466.1:p.Thr467=