Canonical Allele Identifier: CA474566433

Gene: SERPING1

Linked Data

• gnomAD v4: 11-57606029-C-G
• MyVariant Identifiers: chr11:g.57373502C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57606029C>G , CM000673.2:g.57606029C>G	GRCh38
NC_000011.9:g.57373502C>G , CM000673.1:g.57373502C>G	GRCh37
NC_000011.8:g.57130078C>G	NCBI36
NG_009625.1:g.13476C>G , LRG_105:g.13476C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.705C>G MANE Select	ENSP00000278407.4:p.Thr235=
ENST00000528996.2:c.59-5697C>G	ENSP00000431226.2:n.59-5697C>G
ENST00000531605.2:c.*481C>G	ENSP00000503752.1:n.*481C>G
ENST00000619430.2:c.686-379C>G	ENSP00000478572.2:n.686-379C>G
ENST00000676670.1:c.705C>G	ENSP00000504807.1:p.Thr235=
ENST00000676741.1:n.1787C>G
ENST00000677624.1:c.*125C>G	ENSP00000503979.1:n.*125C>G
ENST00000677625.1:c.705C>G	ENSP00000502857.1:p.Thr235=
ENST00000677856.1:n.764C>G
ENST00000677915.1:c.685+3860C>G	ENSP00000503118.1:n.685+3860C>G
ENST00000678533.1:c.*259C>G	ENSP00000503873.1:n.*259C>G
ENST00000678592.1:c.705C>G	ENSP00000504424.1:p.Thr235=
ENST00000278407.8:c.705C>G	ENSP00000278407.4:p.Thr235=
ENST00000340687.10:c.705C>G	ENSP00000341861.6:p.Thr235=
ENST00000378323.8:c.720C>G	ENSP00000367574.4:p.Thr240=
ENST00000378324.6:c.549C>G	ENSP00000367575.2:p.Thr183=
ENST00000403558.1:c.807C>G	ENSP00000384420.1:p.Thr269=
ENST00000531133.5:c.206C>G	ENSP00000435431.1:n.206C>G
ENST00000531605.1:n.552C>G
ENST00000531797.5:c.*54+3860C>G	ENSP00000432554.1:n.*54+3860C>G
ENST00000619430.1:c.348+5854C>G	ENSP00000478572.1:n.348+5854C>G
NM_000062.2:c.705C>G , LRG_105t1:c.705C>G	NP_000053.2:p.Thr235=
NM_001032295.1:c.705C>G	NP_001027466.1:p.Thr235=
NM_000062.3:c.705C>G MANE Select	NP_000053.2:p.Thr235=
NM_001032295.2:c.705C>G	NP_001027466.1:p.Thr235=