Canonical Allele Identifier: CA380690678

Gene: SERPING1

Linked Data

• gnomAD v4: 11-57614442-A-C
• MyVariant Identifiers: chr11:g.57381915A>C (hg19) ; chr11:g.57614442A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614442A>C , CM000673.2:g.57614442A>C	GRCh38
NC_000011.9:g.57381915A>C , CM000673.1:g.57381915A>C	GRCh37
NC_000011.8:g.57138491A>C	NCBI36
NG_009625.1:g.21889A>C , LRG_105:g.21889A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1364A>C MANE Select	ENSP00000278407.4:p.Glu455Ala
ENST00000528996.2:c.*261A>C	ENSP00000431226.2:n.*261A>C
ENST00000531605.2:c.*1140A>C	ENSP00000503752.1:n.*1140A>C
ENST00000619430.2:c.1160A>C	ENSP00000478572.2:p.Glu387Ala
ENST00000676670.1:c.1364A>C	ENSP00000504807.1:p.Glu455Ala
ENST00000676741.1:n.2446A>C
ENST00000677624.1:c.*784A>C	ENSP00000503979.1:n.*784A>C
ENST00000677625.1:c.1310A>C	ENSP00000502857.1:p.Glu437Ala
ENST00000677856.1:n.1617A>C
ENST00000677915.1:c.*261A>C	ENSP00000503118.1:n.*261A>C
ENST00000678533.1:c.*918A>C	ENSP00000503873.1:n.*918A>C
ENST00000678592.1:c.*304A>C	ENSP00000504424.1:n.*304A>C
ENST00000278407.8:c.1364A>C	ENSP00000278407.4:p.Glu455Ala
ENST00000340687.10:c.1253A>C	ENSP00000341861.6:p.Glu418Ala
ENST00000378323.8:c.1379A>C	ENSP00000367574.4:p.Glu460Ala
ENST00000378324.6:c.1208A>C	ENSP00000367575.2:p.Glu403Ala
ENST00000403558.1:c.1493A>C	ENSP00000384420.1:p.Glu498Ala
ENST00000528996.1:c.565A>C	ENSP00000431226.1:n.565A>C
ENST00000530113.1:n.821A>C
ENST00000531133.5:c.865A>C	ENSP00000435431.1:n.865A>C
ENST00000531797.5:c.*389A>C	ENSP00000432554.1:n.*389A>C
ENST00000619430.1:c.495A>C	ENSP00000478572.1:n.495A>C
NM_000062.2:c.1364A>C , LRG_105t1:c.1364A>C	NP_000053.2:p.Glu455Ala
NM_001032295.1:c.1364A>C	NP_001027466.1:p.Glu455Ala
NM_000062.3:c.1364A>C MANE Select	NP_000053.2:p.Glu455Ala
NM_001032295.2:c.1364A>C	NP_001027466.1:p.Glu455Ala