Canonical Allele Identifier: CA474806921

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381982C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614509C>T , CM000673.2:g.57614509C>T	GRCh38
NC_000011.9:g.57381982C>T , CM000673.1:g.57381982C>T	GRCh37
NC_000011.8:g.57138558C>T	NCBI36
NG_009625.1:g.21956C>T , LRG_105:g.21956C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1431C>T MANE Select	ENSP00000278407.4:p.Phe477=
ENST00000528996.2:c.*328C>T	ENSP00000431226.2:n.*328C>T
ENST00000531605.2:c.*1207C>T	ENSP00000503752.1:n.*1207C>T
ENST00000619430.2:c.1227C>T	ENSP00000478572.2:p.Phe409=
ENST00000676670.1:c.1431C>T	ENSP00000504807.1:p.Phe477=
ENST00000676741.1:n.2513C>T
ENST00000677624.1:c.*851C>T	ENSP00000503979.1:n.*851C>T
ENST00000677625.1:c.1377C>T	ENSP00000502857.1:p.Phe459=
ENST00000677856.1:n.1684C>T
ENST00000677915.1:c.*328C>T	ENSP00000503118.1:n.*328C>T
ENST00000678533.1:c.*985C>T	ENSP00000503873.1:n.*985C>T
ENST00000678592.1:c.*371C>T	ENSP00000504424.1:n.*371C>T
ENST00000278407.8:c.1431C>T	ENSP00000278407.4:p.Phe477=
ENST00000340687.10:c.1320C>T	ENSP00000341861.6:p.Phe440=
ENST00000378323.8:c.1446C>T	ENSP00000367574.4:p.Phe482=
ENST00000378324.6:c.1275C>T	ENSP00000367575.2:p.Phe425=
ENST00000403558.1:c.1560C>T	ENSP00000384420.1:p.Phe520=
ENST00000528996.1:c.632C>T	ENSP00000431226.1:n.632C>T
ENST00000530113.1:n.888C>T
ENST00000531133.5:c.932C>T	ENSP00000435431.1:n.932C>T
ENST00000531797.5:c.*456C>T	ENSP00000432554.1:n.*456C>T
ENST00000619430.1:c.562C>T	ENSP00000478572.1:n.562C>T
NM_000062.2:c.1431C>T , LRG_105t1:c.1431C>T	NP_000053.2:p.Phe477=
NM_001032295.1:c.1431C>T	NP_001027466.1:p.Phe477=
NM_000062.3:c.1431C>T MANE Select	NP_000053.2:p.Phe477=
NM_001032295.2:c.1431C>T	NP_001027466.1:p.Phe477=