Canonical Allele Identifier: CA474806957

Gene: SERPING1

Linked Data

• dbSNP Id: rs1365774407
• gnomAD v2: 11-57382021-C-T
• gnomAD v4: 11-57614548-C-T
• MyVariant Identifiers: chr11:g.57382021C>T (hg19) ; chr11:g.57614548C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614548C>T , CM000673.2:g.57614548C>T	GRCh38
NC_000011.9:g.57382021C>T , CM000673.1:g.57382021C>T	GRCh37
NC_000011.8:g.57138597C>T	NCBI36
NG_009625.1:g.21995C>T , LRG_105:g.21995C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1470C>T MANE Select	ENSP00000278407.4:p.Val490=
ENST00000528996.2:c.*367C>T	ENSP00000431226.2:n.*367C>T
ENST00000531605.2:c.*1246C>T	ENSP00000503752.1:n.*1246C>T
ENST00000619430.2:c.1266C>T	ENSP00000478572.2:p.Val422=
ENST00000676670.1:c.1470C>T	ENSP00000504807.1:p.Val490=
ENST00000676741.1:n.2552C>T
ENST00000677624.1:c.*890C>T	ENSP00000503979.1:n.*890C>T
ENST00000677625.1:c.1416C>T	ENSP00000502857.1:p.Val472=
ENST00000677856.1:n.1723C>T
ENST00000677915.1:c.*367C>T	ENSP00000503118.1:n.*367C>T
ENST00000678533.1:c.*1024C>T	ENSP00000503873.1:n.*1024C>T
ENST00000678592.1:c.*410C>T	ENSP00000504424.1:n.*410C>T
ENST00000278407.8:c.1470C>T	ENSP00000278407.4:p.Val490=
ENST00000340687.10:c.1359C>T	ENSP00000341861.6:p.Val453=
ENST00000378323.8:c.1485C>T	ENSP00000367574.4:p.Val495=
ENST00000378324.6:c.1314C>T	ENSP00000367575.2:p.Val438=
ENST00000403558.1:c.1599C>T	ENSP00000384420.1:p.Val533=
ENST00000528996.1:c.671C>T	ENSP00000431226.1:n.671C>T
ENST00000531133.5:c.971C>T	ENSP00000435431.1:n.971C>T
ENST00000531797.5:c.*495C>T	ENSP00000432554.1:n.*495C>T
ENST00000619430.1:c.601C>T	ENSP00000478572.1:n.601C>T
NM_000062.2:c.1470C>T , LRG_105t1:c.1470C>T	NP_000053.2:p.Val490=
NM_001032295.1:c.1470C>T	NP_001027466.1:p.Val490=
NM_000062.3:c.1470C>T MANE Select	NP_000053.2:p.Val490=
NM_001032295.2:c.1470C>T	NP_001027466.1:p.Val490=