Canonical Allele Identifier: CA380702984

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57379311A>G (hg19) ; chr11:g.57611838A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611838A>G , CM000673.2:g.57611838A>G	GRCh38
NC_000011.9:g.57379311A>G , CM000673.1:g.57379311A>G	GRCh37
NC_000011.8:g.57135887A>G	NCBI36
NG_009625.1:g.19285A>G , LRG_105:g.19285A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1151A>G MANE Select	ENSP00000278407.4:p.Glu384Gly
ENST00000528996.2:c.*48A>G	ENSP00000431226.2:n.*48A>G
ENST00000531605.2:c.*927A>G	ENSP00000503752.1:n.*927A>G
ENST00000619430.2:c.947A>G	ENSP00000478572.2:p.Glu316Gly
ENST00000676670.1:c.1151A>G	ENSP00000504807.1:p.Glu384Gly
ENST00000676741.1:n.2233A>G
ENST00000677624.1:c.*571A>G	ENSP00000503979.1:n.*571A>G
ENST00000677625.1:c.1097A>G	ENSP00000502857.1:p.Glu366Gly
ENST00000677856.1:n.1404A>G
ENST00000677915.1:c.*48A>G	ENSP00000503118.1:n.*48A>G
ENST00000678533.1:c.*705A>G	ENSP00000503873.1:n.*705A>G
ENST00000678592.1:c.*91A>G	ENSP00000504424.1:n.*91A>G
ENST00000278407.8:c.1151A>G	ENSP00000278407.4:p.Glu384Gly
ENST00000340687.10:c.1040A>G	ENSP00000341861.6:p.Glu347Gly
ENST00000378323.8:c.1166A>G	ENSP00000367574.4:p.Glu389Gly
ENST00000378324.6:c.995A>G	ENSP00000367575.2:p.Glu332Gly
ENST00000403558.1:c.1280A>G	ENSP00000384420.1:p.Glu427Gly
ENST00000528996.1:c.352A>G	ENSP00000431226.1:n.352A>G
ENST00000530113.1:n.608A>G
ENST00000531133.5:c.652A>G	ENSP00000435431.1:n.652A>G
ENST00000531797.5:c.*176A>G	ENSP00000432554.1:n.*176A>G
ENST00000619430.1:c.349-67A>G	ENSP00000478572.1:n.349-67A>G
NM_000062.2:c.1151A>G , LRG_105t1:c.1151A>G	NP_000053.2:p.Glu384Gly
NM_001032295.1:c.1151A>G	NP_001027466.1:p.Glu384Gly
NM_000062.3:c.1151A>G MANE Select	NP_000053.2:p.Glu384Gly
NM_001032295.2:c.1151A>G	NP_001027466.1:p.Glu384Gly