Canonical Allele Identifier: CA380690834

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381992C>A (hg19) ; chr11:g.57614519C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614519C>A , CM000673.2:g.57614519C>A	GRCh38
NC_000011.9:g.57381992C>A , CM000673.1:g.57381992C>A	GRCh37
NC_000011.8:g.57138568C>A	NCBI36
NG_009625.1:g.21966C>A , LRG_105:g.21966C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1441C>A MANE Select	ENSP00000278407.4:p.Leu481Ile
ENST00000528996.2:c.*338C>A	ENSP00000431226.2:n.*338C>A
ENST00000531605.2:c.*1217C>A	ENSP00000503752.1:n.*1217C>A
ENST00000619430.2:c.1237C>A	ENSP00000478572.2:p.Leu413Ile
ENST00000676670.1:c.1441C>A	ENSP00000504807.1:p.Leu481Ile
ENST00000676741.1:n.2523C>A
ENST00000677624.1:c.*861C>A	ENSP00000503979.1:n.*861C>A
ENST00000677625.1:c.1387C>A	ENSP00000502857.1:p.Leu463Ile
ENST00000677856.1:n.1694C>A
ENST00000677915.1:c.*338C>A	ENSP00000503118.1:n.*338C>A
ENST00000678533.1:c.*995C>A	ENSP00000503873.1:n.*995C>A
ENST00000678592.1:c.*381C>A	ENSP00000504424.1:n.*381C>A
ENST00000278407.8:c.1441C>A	ENSP00000278407.4:p.Leu481Ile
ENST00000340687.10:c.1330C>A	ENSP00000341861.6:p.Leu444Ile
ENST00000378323.8:c.1456C>A	ENSP00000367574.4:p.Leu486Ile
ENST00000378324.6:c.1285C>A	ENSP00000367575.2:p.Leu429Ile
ENST00000403558.1:c.1570C>A	ENSP00000384420.1:p.Leu524Ile
ENST00000528996.1:c.642C>A	ENSP00000431226.1:n.642C>A
ENST00000530113.1:n.898C>A
ENST00000531133.5:c.942C>A	ENSP00000435431.1:n.942C>A
ENST00000531797.5:c.*466C>A	ENSP00000432554.1:n.*466C>A
ENST00000619430.1:c.572C>A	ENSP00000478572.1:n.572C>A
NM_000062.2:c.1441C>A , LRG_105t1:c.1441C>A	NP_000053.2:p.Leu481Ile
NM_001032295.1:c.1441C>A	NP_001027466.1:p.Leu481Ile
NM_000062.3:c.1441C>A MANE Select	NP_000053.2:p.Leu481Ile
NM_001032295.2:c.1441C>A	NP_001027466.1:p.Leu481Ile