Canonical Allele Identifier: CA380703436

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57379379C>G (hg19) ; chr11:g.57611906C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611906C>G , CM000673.2:g.57611906C>G	GRCh38
NC_000011.9:g.57379379C>G , CM000673.1:g.57379379C>G	GRCh37
NC_000011.8:g.57135955C>G	NCBI36
NG_009625.1:g.19353C>G , LRG_105:g.19353C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1219C>G MANE Select	ENSP00000278407.4:p.Gln407Glu
ENST00000528996.2:c.*116C>G	ENSP00000431226.2:n.*116C>G
ENST00000531605.2:c.*995C>G	ENSP00000503752.1:n.*995C>G
ENST00000619430.2:c.1015C>G	ENSP00000478572.2:p.Gln339Glu
ENST00000676670.1:c.1219C>G	ENSP00000504807.1:p.Gln407Glu
ENST00000676741.1:n.2301C>G
ENST00000677624.1:c.*639C>G	ENSP00000503979.1:n.*639C>G
ENST00000677625.1:c.1165C>G	ENSP00000502857.1:p.Gln389Glu
ENST00000677856.1:n.1472C>G
ENST00000677915.1:c.*116C>G	ENSP00000503118.1:n.*116C>G
ENST00000678533.1:c.*773C>G	ENSP00000503873.1:n.*773C>G
ENST00000678592.1:c.*159C>G	ENSP00000504424.1:n.*159C>G
ENST00000278407.8:c.1219C>G	ENSP00000278407.4:p.Gln407Glu
ENST00000340687.10:c.1108C>G	ENSP00000341861.6:p.Gln370Glu
ENST00000378323.8:c.1234C>G	ENSP00000367574.4:p.Gln412Glu
ENST00000378324.6:c.1063C>G	ENSP00000367575.2:p.Gln355Glu
ENST00000403558.1:c.1348C>G	ENSP00000384420.1:p.Gln450Glu
ENST00000528996.1:c.420C>G	ENSP00000431226.1:n.420C>G
ENST00000530113.1:n.676C>G
ENST00000531133.5:c.720C>G	ENSP00000435431.1:n.720C>G
ENST00000531797.5:c.*244C>G	ENSP00000432554.1:n.*244C>G
ENST00000619430.1:c.350C>G	ENSP00000478572.1:p.Pro117Arg
NM_000062.2:c.1219C>G , LRG_105t1:c.1219C>G	NP_000053.2:p.Gln407Glu
NM_001032295.1:c.1219C>G	NP_001027466.1:p.Gln407Glu
NM_000062.3:c.1219C>G MANE Select	NP_000053.2:p.Gln407Glu
NM_001032295.2:c.1219C>G	NP_001027466.1:p.Gln407Glu