Canonical Allele Identifier: CA380690929

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57382031C>G (hg19) ; chr11:g.57614558C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614558C>G , CM000673.2:g.57614558C>G	GRCh38
NC_000011.9:g.57382031C>G , CM000673.1:g.57382031C>G	GRCh37
NC_000011.8:g.57138607C>G	NCBI36
NG_009625.1:g.22005C>G , LRG_105:g.22005C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1480C>G MANE Select	ENSP00000278407.4:p.Arg494Gly
ENST00000528996.2:c.*377C>G	ENSP00000431226.2:n.*377C>G
ENST00000531605.2:c.*1256C>G	ENSP00000503752.1:n.*1256C>G
ENST00000619430.2:c.1276C>G	ENSP00000478572.2:p.Arg426Gly
ENST00000676670.1:c.1480C>G	ENSP00000504807.1:p.Arg494Gly
ENST00000676741.1:n.2562C>G
ENST00000677624.1:c.*900C>G	ENSP00000503979.1:n.*900C>G
ENST00000677625.1:c.1426C>G	ENSP00000502857.1:p.Arg476Gly
ENST00000677856.1:n.1733C>G
ENST00000677915.1:c.*377C>G	ENSP00000503118.1:n.*377C>G
ENST00000678533.1:c.*1034C>G	ENSP00000503873.1:n.*1034C>G
ENST00000678592.1:c.*420C>G	ENSP00000504424.1:n.*420C>G
ENST00000278407.8:c.1480C>G	ENSP00000278407.4:p.Arg494Gly
ENST00000340687.10:c.1369C>G	ENSP00000341861.6:p.Arg457Gly
ENST00000378323.8:c.1495C>G	ENSP00000367574.4:p.Arg499Gly
ENST00000378324.6:c.1324C>G	ENSP00000367575.2:p.Arg442Gly
ENST00000403558.1:c.1609C>G	ENSP00000384420.1:p.Arg537Gly
ENST00000528996.1:c.681C>G	ENSP00000431226.1:n.681C>G
ENST00000531133.5:c.981C>G	ENSP00000435431.1:n.981C>G
ENST00000531797.5:c.*505C>G	ENSP00000432554.1:n.*505C>G
ENST00000619430.1:c.611C>G	ENSP00000478572.1:n.611C>G
NM_000062.2:c.1480C>G , LRG_105t1:c.1480C>G	NP_000053.2:p.Arg494Gly
NM_001032295.1:c.1480C>G	NP_001027466.1:p.Arg494Gly
NM_000062.3:c.1480C>G MANE Select	NP_000053.2:p.Arg494Gly
NM_001032295.2:c.1480C>G	NP_001027466.1:p.Arg494Gly