Canonical Allele Identifier: CA380690895

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57382015C>G (hg19) ; chr11:g.57614542C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614542C>G , CM000673.2:g.57614542C>G	GRCh38
NC_000011.9:g.57382015C>G , CM000673.1:g.57382015C>G	GRCh37
NC_000011.8:g.57138591C>G	NCBI36
NG_009625.1:g.21989C>G , LRG_105:g.21989C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1464C>G MANE Select	ENSP00000278407.4:p.Phe488Leu
ENST00000528996.2:c.*361C>G	ENSP00000431226.2:n.*361C>G
ENST00000531605.2:c.*1240C>G	ENSP00000503752.1:n.*1240C>G
ENST00000619430.2:c.1260C>G	ENSP00000478572.2:p.Phe420Leu
ENST00000676670.1:c.1464C>G	ENSP00000504807.1:p.Phe488Leu
ENST00000676741.1:n.2546C>G
ENST00000677624.1:c.*884C>G	ENSP00000503979.1:n.*884C>G
ENST00000677625.1:c.1410C>G	ENSP00000502857.1:p.Phe470Leu
ENST00000677856.1:n.1717C>G
ENST00000677915.1:c.*361C>G	ENSP00000503118.1:n.*361C>G
ENST00000678533.1:c.*1018C>G	ENSP00000503873.1:n.*1018C>G
ENST00000678592.1:c.*404C>G	ENSP00000504424.1:n.*404C>G
ENST00000278407.8:c.1464C>G	ENSP00000278407.4:p.Phe488Leu
ENST00000340687.10:c.1353C>G	ENSP00000341861.6:p.Phe451Leu
ENST00000378323.8:c.1479C>G	ENSP00000367574.4:p.Phe493Leu
ENST00000378324.6:c.1308C>G	ENSP00000367575.2:p.Phe436Leu
ENST00000403558.1:c.1593C>G	ENSP00000384420.1:p.Phe531Leu
ENST00000528996.1:c.665C>G	ENSP00000431226.1:n.665C>G
ENST00000531133.5:c.965C>G	ENSP00000435431.1:n.965C>G
ENST00000531797.5:c.*489C>G	ENSP00000432554.1:n.*489C>G
ENST00000619430.1:c.595C>G	ENSP00000478572.1:n.595C>G
NM_000062.2:c.1464C>G , LRG_105t1:c.1464C>G	NP_000053.2:p.Phe488Leu
NM_001032295.1:c.1464C>G	NP_001027466.1:p.Phe488Leu
NM_000062.3:c.1464C>G MANE Select	NP_000053.2:p.Phe488Leu
NM_001032295.2:c.1464C>G	NP_001027466.1:p.Phe488Leu