Canonical Allele Identifier: CA380702492

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57379229A>G (hg19) ; chr11:g.57611756A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611756A>G , CM000673.2:g.57611756A>G	GRCh38
NC_000011.9:g.57379229A>G , CM000673.1:g.57379229A>G	GRCh37
NC_000011.8:g.57135805A>G	NCBI36
NG_009625.1:g.19203A>G , LRG_105:g.19203A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.1069A>G MANE Select	ENSP00000278407.4:p.Ile357Val
ENST00000528996.2:c.89A>G	ENSP00000431226.2:p.Asp30Gly
ENST00000531605.2:c.*845A>G	ENSP00000503752.1:n.*845A>G
ENST00000619430.2:c.865A>G	ENSP00000478572.2:p.Ile289Val
ENST00000676670.1:c.1069A>G	ENSP00000504807.1:p.Ile357Val
ENST00000676741.1:n.2151A>G
ENST00000677624.1:c.*489A>G	ENSP00000503979.1:n.*489A>G
ENST00000677625.1:c.1030-15A>G	ENSP00000502857.1:n.1030-15A>G
ENST00000677856.1:n.1322A>G
ENST00000677915.1:c.725A>G	ENSP00000503118.1:p.Asp242Gly
ENST00000678533.1:c.*623A>G	ENSP00000503873.1:n.*623A>G
ENST00000678592.1:c.*9A>G	ENSP00000504424.1:n.*9A>G
ENST00000278407.8:c.1069A>G	ENSP00000278407.4:p.Ile357Val
ENST00000340687.10:c.1030-72A>G	ENSP00000341861.6:n.1030-72A>G
ENST00000378323.8:c.1084A>G	ENSP00000367574.4:p.Ile362Val
ENST00000378324.6:c.913A>G	ENSP00000367575.2:p.Ile305Val
ENST00000403558.1:c.1198A>G	ENSP00000384420.1:p.Ile400Val
ENST00000528996.1:c.270A>G	ENSP00000431226.1:n.270A>G
ENST00000530113.1:n.526A>G
ENST00000531133.5:c.570A>G	ENSP00000435431.1:n.570A>G
ENST00000531797.5:c.*94A>G	ENSP00000432554.1:n.*94A>G
ENST00000619430.1:c.349-149A>G	ENSP00000478572.1:n.349-149A>G
NM_000062.2:c.1069A>G , LRG_105t1:c.1069A>G	NP_000053.2:p.Ile357Val
NM_001032295.1:c.1069A>G	NP_001027466.1:p.Ile357Val
NM_000062.3:c.1069A>G MANE Select	NP_000053.2:p.Ile357Val
NM_001032295.2:c.1069A>G	NP_001027466.1:p.Ile357Val