Canonical Allele Identifier: CA474806886

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381955G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614482G>T , CM000673.2:g.57614482G>T	GRCh38
NC_000011.9:g.57381955G>T , CM000673.1:g.57381955G>T	GRCh37
NC_000011.8:g.57138531G>T	NCBI36
NG_009625.1:g.21929G>T , LRG_105:g.21929G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1404G>T MANE Select	ENSP00000278407.4:p.Leu468=
ENST00000528996.2:c.*301G>T	ENSP00000431226.2:n.*301G>T
ENST00000531605.2:c.*1180G>T	ENSP00000503752.1:n.*1180G>T
ENST00000619430.2:c.1200G>T	ENSP00000478572.2:p.Leu400=
ENST00000676670.1:c.1404G>T	ENSP00000504807.1:p.Leu468=
ENST00000676741.1:n.2486G>T
ENST00000677624.1:c.*824G>T	ENSP00000503979.1:n.*824G>T
ENST00000677625.1:c.1350G>T	ENSP00000502857.1:p.Leu450=
ENST00000677856.1:n.1657G>T
ENST00000677915.1:c.*301G>T	ENSP00000503118.1:n.*301G>T
ENST00000678533.1:c.*958G>T	ENSP00000503873.1:n.*958G>T
ENST00000678592.1:c.*344G>T	ENSP00000504424.1:n.*344G>T
ENST00000278407.8:c.1404G>T	ENSP00000278407.4:p.Leu468=
ENST00000340687.10:c.1293G>T	ENSP00000341861.6:p.Leu431=
ENST00000378323.8:c.1419G>T	ENSP00000367574.4:p.Leu473=
ENST00000378324.6:c.1248G>T	ENSP00000367575.2:p.Leu416=
ENST00000403558.1:c.1533G>T	ENSP00000384420.1:p.Leu511=
ENST00000528996.1:c.605G>T	ENSP00000431226.1:n.605G>T
ENST00000530113.1:n.861G>T
ENST00000531133.5:c.905G>T	ENSP00000435431.1:n.905G>T
ENST00000531797.5:c.*429G>T	ENSP00000432554.1:n.*429G>T
ENST00000619430.1:c.535G>T	ENSP00000478572.1:n.535G>T
NM_000062.2:c.1404G>T , LRG_105t1:c.1404G>T	NP_000053.2:p.Leu468=
NM_001032295.1:c.1404G>T	NP_001027466.1:p.Leu468=
NM_000062.3:c.1404G>T MANE Select	NP_000053.2:p.Leu468=
NM_001032295.2:c.1404G>T	NP_001027466.1:p.Leu468=