Canonical Allele Identifier: CA474806877

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381949C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614476C>T , CM000673.2:g.57614476C>T	GRCh38
NC_000011.9:g.57381949C>T , CM000673.1:g.57381949C>T	GRCh37
NC_000011.8:g.57138525C>T	NCBI36
NG_009625.1:g.21923C>T , LRG_105:g.21923C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1398C>T MANE Select	ENSP00000278407.4:p.Arg466=
ENST00000528996.2:c.*295C>T	ENSP00000431226.2:n.*295C>T
ENST00000531605.2:c.*1174C>T	ENSP00000503752.1:n.*1174C>T
ENST00000619430.2:c.1194C>T	ENSP00000478572.2:p.Arg398=
ENST00000676670.1:c.1398C>T	ENSP00000504807.1:p.Arg466=
ENST00000676741.1:n.2480C>T
ENST00000677624.1:c.*818C>T	ENSP00000503979.1:n.*818C>T
ENST00000677625.1:c.1344C>T	ENSP00000502857.1:p.Arg448=
ENST00000677856.1:n.1651C>T
ENST00000677915.1:c.*295C>T	ENSP00000503118.1:n.*295C>T
ENST00000678533.1:c.*952C>T	ENSP00000503873.1:n.*952C>T
ENST00000678592.1:c.*338C>T	ENSP00000504424.1:n.*338C>T
ENST00000278407.8:c.1398C>T	ENSP00000278407.4:p.Arg466=
ENST00000340687.10:c.1287C>T	ENSP00000341861.6:p.Arg429=
ENST00000378323.8:c.1413C>T	ENSP00000367574.4:p.Arg471=
ENST00000378324.6:c.1242C>T	ENSP00000367575.2:p.Arg414=
ENST00000403558.1:c.1527C>T	ENSP00000384420.1:p.Arg509=
ENST00000528996.1:c.599C>T	ENSP00000431226.1:n.599C>T
ENST00000530113.1:n.855C>T
ENST00000531133.5:c.899C>T	ENSP00000435431.1:n.899C>T
ENST00000531797.5:c.*423C>T	ENSP00000432554.1:n.*423C>T
ENST00000619430.1:c.529C>T	ENSP00000478572.1:n.529C>T
NM_000062.2:c.1398C>T , LRG_105t1:c.1398C>T	NP_000053.2:p.Arg466=
NM_001032295.1:c.1398C>T	NP_001027466.1:p.Arg466=
NM_000062.3:c.1398C>T MANE Select	NP_000053.2:p.Arg466=
NM_001032295.2:c.1398C>T	NP_001027466.1:p.Arg466=