Canonical Allele Identifier: CA380690334

Gene: SERPING1

Linked Data

• gnomAD v4: 11-57614370-C-T
• MyVariant Identifiers: chr11:g.57381843C>T (hg19) ; chr11:g.57614370C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614370C>T , CM000673.2:g.57614370C>T	GRCh38
NC_000011.9:g.57381843C>T , CM000673.1:g.57381843C>T	GRCh37
NC_000011.8:g.57138419C>T	NCBI36
NG_009625.1:g.21817C>T , LRG_105:g.21817C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.1292C>T MANE Select	ENSP00000278407.4:p.Thr431Ile
ENST00000528996.2:c.*189C>T	ENSP00000431226.2:n.*189C>T
ENST00000531605.2:c.*1068C>T	ENSP00000503752.1:n.*1068C>T
ENST00000619430.2:c.1088C>T	ENSP00000478572.2:p.Thr363Ile
ENST00000676670.1:c.1292C>T	ENSP00000504807.1:p.Thr431Ile
ENST00000676741.1:n.2374C>T
ENST00000677624.1:c.*712C>T	ENSP00000503979.1:n.*712C>T
ENST00000677625.1:c.1238C>T	ENSP00000502857.1:p.Thr413Ile
ENST00000677856.1:n.1545C>T
ENST00000677915.1:c.*189C>T	ENSP00000503118.1:n.*189C>T
ENST00000678533.1:c.*846C>T	ENSP00000503873.1:n.*846C>T
ENST00000678592.1:c.*232C>T	ENSP00000504424.1:n.*232C>T
ENST00000278407.8:c.1292C>T	ENSP00000278407.4:p.Thr431Ile
ENST00000340687.10:c.1181C>T	ENSP00000341861.6:p.Thr394Ile
ENST00000378323.8:c.1307C>T	ENSP00000367574.4:p.Thr436Ile
ENST00000378324.6:c.1136C>T	ENSP00000367575.2:p.Thr379Ile
ENST00000403558.1:c.1421C>T	ENSP00000384420.1:p.Thr474Ile
ENST00000528996.1:c.493C>T	ENSP00000431226.1:n.493C>T
ENST00000530113.1:n.749C>T
ENST00000531133.5:c.793C>T	ENSP00000435431.1:n.793C>T
ENST00000531797.5:c.*317C>T	ENSP00000432554.1:n.*317C>T
ENST00000619430.1:c.423C>T	ENSP00000478572.1:n.423C>T
NM_000062.2:c.1292C>T , LRG_105t1:c.1292C>T	NP_000053.2:p.Thr431Ile
NM_001032295.1:c.1292C>T	NP_001027466.1:p.Thr431Ile
NM_000062.3:c.1292C>T MANE Select	NP_000053.2:p.Thr431Ile
NM_001032295.2:c.1292C>T	NP_001027466.1:p.Thr431Ile