Canonical Allele Identifier: CA380690699

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381924C>A (hg19) ; chr11:g.57614451C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614451C>A , CM000673.2:g.57614451C>A	GRCh38
NC_000011.9:g.57381924C>A , CM000673.1:g.57381924C>A	GRCh37
NC_000011.8:g.57138500C>A	NCBI36
NG_009625.1:g.21898C>A , LRG_105:g.21898C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1373C>A MANE Select	ENSP00000278407.4:p.Ala458Glu
ENST00000528996.2:c.*270C>A	ENSP00000431226.2:n.*270C>A
ENST00000531605.2:c.*1149C>A	ENSP00000503752.1:n.*1149C>A
ENST00000619430.2:c.1169C>A	ENSP00000478572.2:p.Ala390Glu
ENST00000676670.1:c.1373C>A	ENSP00000504807.1:p.Ala458Glu
ENST00000676741.1:n.2455C>A
ENST00000677624.1:c.*793C>A	ENSP00000503979.1:n.*793C>A
ENST00000677625.1:c.1319C>A	ENSP00000502857.1:p.Ala440Glu
ENST00000677856.1:n.1626C>A
ENST00000677915.1:c.*270C>A	ENSP00000503118.1:n.*270C>A
ENST00000678533.1:c.*927C>A	ENSP00000503873.1:n.*927C>A
ENST00000678592.1:c.*313C>A	ENSP00000504424.1:n.*313C>A
ENST00000278407.8:c.1373C>A	ENSP00000278407.4:p.Ala458Glu
ENST00000340687.10:c.1262C>A	ENSP00000341861.6:p.Ala421Glu
ENST00000378323.8:c.1388C>A	ENSP00000367574.4:p.Ala463Glu
ENST00000378324.6:c.1217C>A	ENSP00000367575.2:p.Ala406Glu
ENST00000403558.1:c.1502C>A	ENSP00000384420.1:p.Ala501Glu
ENST00000528996.1:c.574C>A	ENSP00000431226.1:n.574C>A
ENST00000530113.1:n.830C>A
ENST00000531133.5:c.874C>A	ENSP00000435431.1:n.874C>A
ENST00000531797.5:c.*398C>A	ENSP00000432554.1:n.*398C>A
ENST00000619430.1:c.504C>A	ENSP00000478572.1:n.504C>A
NM_000062.2:c.1373C>A , LRG_105t1:c.1373C>A	NP_000053.2:p.Ala458Glu
NM_001032295.1:c.1373C>A	NP_001027466.1:p.Ala458Glu
NM_000062.3:c.1373C>A MANE Select	NP_000053.2:p.Ala458Glu
NM_001032295.2:c.1373C>A	NP_001027466.1:p.Ala458Glu