Canonical Allele Identifier: CA380690754

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381956C>G (hg19) ; chr11:g.57614483C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614483C>G , CM000673.2:g.57614483C>G	GRCh38
NC_000011.9:g.57381956C>G , CM000673.1:g.57381956C>G	GRCh37
NC_000011.8:g.57138532C>G	NCBI36
NG_009625.1:g.21930C>G , LRG_105:g.21930C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1405C>G MANE Select	ENSP00000278407.4:p.Leu469Val
ENST00000528996.2:c.*302C>G	ENSP00000431226.2:n.*302C>G
ENST00000531605.2:c.*1181C>G	ENSP00000503752.1:n.*1181C>G
ENST00000619430.2:c.1201C>G	ENSP00000478572.2:p.Leu401Val
ENST00000676670.1:c.1405C>G	ENSP00000504807.1:p.Leu469Val
ENST00000676741.1:n.2487C>G
ENST00000677624.1:c.*825C>G	ENSP00000503979.1:n.*825C>G
ENST00000677625.1:c.1351C>G	ENSP00000502857.1:p.Leu451Val
ENST00000677856.1:n.1658C>G
ENST00000677915.1:c.*302C>G	ENSP00000503118.1:n.*302C>G
ENST00000678533.1:c.*959C>G	ENSP00000503873.1:n.*959C>G
ENST00000678592.1:c.*345C>G	ENSP00000504424.1:n.*345C>G
ENST00000278407.8:c.1405C>G	ENSP00000278407.4:p.Leu469Val
ENST00000340687.10:c.1294C>G	ENSP00000341861.6:p.Leu432Val
ENST00000378323.8:c.1420C>G	ENSP00000367574.4:p.Leu474Val
ENST00000378324.6:c.1249C>G	ENSP00000367575.2:p.Leu417Val
ENST00000403558.1:c.1534C>G	ENSP00000384420.1:p.Leu512Val
ENST00000528996.1:c.606C>G	ENSP00000431226.1:n.606C>G
ENST00000530113.1:n.862C>G
ENST00000531133.5:c.906C>G	ENSP00000435431.1:n.906C>G
ENST00000531797.5:c.*430C>G	ENSP00000432554.1:n.*430C>G
ENST00000619430.1:c.536C>G	ENSP00000478572.1:n.536C>G
NM_000062.2:c.1405C>G , LRG_105t1:c.1405C>G	NP_000053.2:p.Leu469Val
NM_001032295.1:c.1405C>G	NP_001027466.1:p.Leu469Val
NM_000062.3:c.1405C>G MANE Select	NP_000053.2:p.Leu469Val
NM_001032295.2:c.1405C>G	NP_001027466.1:p.Leu469Val