Canonical Allele Identifier: CA380702911

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57379301G>A (hg19) ; chr11:g.57611828G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611828G>A , CM000673.2:g.57611828G>A	GRCh38
NC_000011.9:g.57379301G>A , CM000673.1:g.57379301G>A	GRCh37
NC_000011.8:g.57135877G>A	NCBI36
NG_009625.1:g.19275G>A , LRG_105:g.19275G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1141G>A MANE Select	ENSP00000278407.4:p.Ala381Thr
ENST00000528996.2:c.*38G>A	ENSP00000431226.2:n.*38G>A
ENST00000531605.2:c.*917G>A	ENSP00000503752.1:n.*917G>A
ENST00000619430.2:c.937G>A	ENSP00000478572.2:p.Ala313Thr
ENST00000676670.1:c.1141G>A	ENSP00000504807.1:p.Ala381Thr
ENST00000676741.1:n.2223G>A
ENST00000677624.1:c.*561G>A	ENSP00000503979.1:n.*561G>A
ENST00000677625.1:c.1087G>A	ENSP00000502857.1:p.Ala363Thr
ENST00000677856.1:n.1394G>A
ENST00000677915.1:c.*38G>A	ENSP00000503118.1:n.*38G>A
ENST00000678533.1:c.*695G>A	ENSP00000503873.1:n.*695G>A
ENST00000678592.1:c.*81G>A	ENSP00000504424.1:n.*81G>A
ENST00000278407.8:c.1141G>A	ENSP00000278407.4:p.Ala381Thr
ENST00000340687.10:c.1030G>A	ENSP00000341861.6:p.Ala344Thr
ENST00000378323.8:c.1156G>A	ENSP00000367574.4:p.Ala386Thr
ENST00000378324.6:c.985G>A	ENSP00000367575.2:p.Ala329Thr
ENST00000403558.1:c.1270G>A	ENSP00000384420.1:p.Ala424Thr
ENST00000528996.1:c.342G>A	ENSP00000431226.1:n.342G>A
ENST00000530113.1:n.598G>A
ENST00000531133.5:c.642G>A	ENSP00000435431.1:n.642G>A
ENST00000531797.5:c.*166G>A	ENSP00000432554.1:n.*166G>A
ENST00000619430.1:c.349-77G>A	ENSP00000478572.1:n.349-77G>A
NM_000062.2:c.1141G>A , LRG_105t1:c.1141G>A	NP_000053.2:p.Ala381Thr
NM_001032295.1:c.1141G>A	NP_001027466.1:p.Ala381Thr
NM_000062.3:c.1141G>A MANE Select	NP_000053.2:p.Ala381Thr
NM_001032295.2:c.1141G>A	NP_001027466.1:p.Ala381Thr