Canonical Allele Identifier: CA380690329

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381842A>G (hg19) ; chr11:g.57614369A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614369A>G , CM000673.2:g.57614369A>G	GRCh38
NC_000011.9:g.57381842A>G , CM000673.1:g.57381842A>G	GRCh37
NC_000011.8:g.57138418A>G	NCBI36
NG_009625.1:g.21816A>G , LRG_105:g.21816A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.1291A>G MANE Select	ENSP00000278407.4:p.Thr431Ala
ENST00000528996.2:c.*188A>G	ENSP00000431226.2:n.*188A>G
ENST00000531605.2:c.*1067A>G	ENSP00000503752.1:n.*1067A>G
ENST00000619430.2:c.1087A>G	ENSP00000478572.2:p.Thr363Ala
ENST00000676670.1:c.1291A>G	ENSP00000504807.1:p.Thr431Ala
ENST00000676741.1:n.2373A>G
ENST00000677624.1:c.*711A>G	ENSP00000503979.1:n.*711A>G
ENST00000677625.1:c.1237A>G	ENSP00000502857.1:p.Thr413Ala
ENST00000677856.1:n.1544A>G
ENST00000677915.1:c.*188A>G	ENSP00000503118.1:n.*188A>G
ENST00000678533.1:c.*845A>G	ENSP00000503873.1:n.*845A>G
ENST00000678592.1:c.*231A>G	ENSP00000504424.1:n.*231A>G
ENST00000278407.8:c.1291A>G	ENSP00000278407.4:p.Thr431Ala
ENST00000340687.10:c.1180A>G	ENSP00000341861.6:p.Thr394Ala
ENST00000378323.8:c.1306A>G	ENSP00000367574.4:p.Thr436Ala
ENST00000378324.6:c.1135A>G	ENSP00000367575.2:p.Thr379Ala
ENST00000403558.1:c.1420A>G	ENSP00000384420.1:p.Thr474Ala
ENST00000528996.1:c.492A>G	ENSP00000431226.1:n.492A>G
ENST00000530113.1:n.748A>G
ENST00000531133.5:c.792A>G	ENSP00000435431.1:n.792A>G
ENST00000531797.5:c.*316A>G	ENSP00000432554.1:n.*316A>G
ENST00000619430.1:c.422A>G	ENSP00000478572.1:n.422A>G
NM_000062.2:c.1291A>G , LRG_105t1:c.1291A>G	NP_000053.2:p.Thr431Ala
NM_001032295.1:c.1291A>G	NP_001027466.1:p.Thr431Ala
NM_000062.3:c.1291A>G MANE Select	NP_000053.2:p.Thr431Ala
NM_001032295.2:c.1291A>G	NP_001027466.1:p.Thr431Ala