Canonical Allele Identifier: CA380690854

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381999A>G (hg19) ; chr11:g.57614526A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614526A>G , CM000673.2:g.57614526A>G	GRCh38
NC_000011.9:g.57381999A>G , CM000673.1:g.57381999A>G	GRCh37
NC_000011.8:g.57138575A>G	NCBI36
NG_009625.1:g.21973A>G , LRG_105:g.21973A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1448A>G MANE Select	ENSP00000278407.4:p.Asp483Gly
ENST00000528996.2:c.*345A>G	ENSP00000431226.2:n.*345A>G
ENST00000531605.2:c.*1224A>G	ENSP00000503752.1:n.*1224A>G
ENST00000619430.2:c.1244A>G	ENSP00000478572.2:p.Asp415Gly
ENST00000676670.1:c.1448A>G	ENSP00000504807.1:p.Asp483Gly
ENST00000676741.1:n.2530A>G
ENST00000677624.1:c.*868A>G	ENSP00000503979.1:n.*868A>G
ENST00000677625.1:c.1394A>G	ENSP00000502857.1:p.Asp465Gly
ENST00000677856.1:n.1701A>G
ENST00000677915.1:c.*345A>G	ENSP00000503118.1:n.*345A>G
ENST00000678533.1:c.*1002A>G	ENSP00000503873.1:n.*1002A>G
ENST00000678592.1:c.*388A>G	ENSP00000504424.1:n.*388A>G
ENST00000278407.8:c.1448A>G	ENSP00000278407.4:p.Asp483Gly
ENST00000340687.10:c.1337A>G	ENSP00000341861.6:p.Asp446Gly
ENST00000378323.8:c.1463A>G	ENSP00000367574.4:p.Asp488Gly
ENST00000378324.6:c.1292A>G	ENSP00000367575.2:p.Asp431Gly
ENST00000403558.1:c.1577A>G	ENSP00000384420.1:p.Asp526Gly
ENST00000528996.1:c.649A>G	ENSP00000431226.1:n.649A>G
ENST00000530113.1:n.905A>G
ENST00000531133.5:c.949A>G	ENSP00000435431.1:n.949A>G
ENST00000531797.5:c.*473A>G	ENSP00000432554.1:n.*473A>G
ENST00000619430.1:c.579A>G	ENSP00000478572.1:n.579A>G
NM_000062.2:c.1448A>G , LRG_105t1:c.1448A>G	NP_000053.2:p.Asp483Gly
NM_001032295.1:c.1448A>G	NP_001027466.1:p.Asp483Gly
NM_000062.3:c.1448A>G MANE Select	NP_000053.2:p.Asp483Gly
NM_001032295.2:c.1448A>G	NP_001027466.1:p.Asp483Gly