Canonical Allele Identifier: CA380703187

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57379334C>G (hg19) ; chr11:g.57611861C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611861C>G , CM000673.2:g.57611861C>G	GRCh38
NC_000011.9:g.57379334C>G , CM000673.1:g.57379334C>G	GRCh37
NC_000011.8:g.57135910C>G	NCBI36
NG_009625.1:g.19308C>G , LRG_105:g.19308C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.1174C>G MANE Select	ENSP00000278407.4:p.Gln392Glu
ENST00000528996.2:c.*71C>G	ENSP00000431226.2:n.*71C>G
ENST00000531605.2:c.*950C>G	ENSP00000503752.1:n.*950C>G
ENST00000619430.2:c.970C>G	ENSP00000478572.2:p.Gln324Glu
ENST00000676670.1:c.1174C>G	ENSP00000504807.1:p.Gln392Glu
ENST00000676741.1:n.2256C>G
ENST00000677624.1:c.*594C>G	ENSP00000503979.1:n.*594C>G
ENST00000677625.1:c.1120C>G	ENSP00000502857.1:p.Gln374Glu
ENST00000677856.1:n.1427C>G
ENST00000677915.1:c.*71C>G	ENSP00000503118.1:n.*71C>G
ENST00000678533.1:c.*728C>G	ENSP00000503873.1:n.*728C>G
ENST00000678592.1:c.*114C>G	ENSP00000504424.1:n.*114C>G
ENST00000278407.8:c.1174C>G	ENSP00000278407.4:p.Gln392Glu
ENST00000340687.10:c.1063C>G	ENSP00000341861.6:p.Gln355Glu
ENST00000378323.8:c.1189C>G	ENSP00000367574.4:p.Gln397Glu
ENST00000378324.6:c.1018C>G	ENSP00000367575.2:p.Gln340Glu
ENST00000403558.1:c.1303C>G	ENSP00000384420.1:p.Gln435Glu
ENST00000528996.1:c.375C>G	ENSP00000431226.1:n.375C>G
ENST00000530113.1:n.631C>G
ENST00000531133.5:c.675C>G	ENSP00000435431.1:n.675C>G
ENST00000531797.5:c.*199C>G	ENSP00000432554.1:n.*199C>G
ENST00000619430.1:c.349-44C>G	ENSP00000478572.1:n.349-44C>G
NM_000062.2:c.1174C>G , LRG_105t1:c.1174C>G	NP_000053.2:p.Gln392Glu
NM_001032295.1:c.1174C>G	NP_001027466.1:p.Gln392Glu
NM_000062.3:c.1174C>G MANE Select	NP_000053.2:p.Gln392Glu
NM_001032295.2:c.1174C>G	NP_001027466.1:p.Gln392Glu