Canonical Allele Identifier: CA380703180

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57379333C>G (hg19) ; chr11:g.57611860C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611860C>G , CM000673.2:g.57611860C>G	GRCh38
NC_000011.9:g.57379333C>G , CM000673.1:g.57379333C>G	GRCh37
NC_000011.8:g.57135909C>G	NCBI36
NG_009625.1:g.19307C>G , LRG_105:g.19307C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1173C>G MANE Select	ENSP00000278407.4:p.Phe391Leu
ENST00000528996.2:c.*70C>G	ENSP00000431226.2:n.*70C>G
ENST00000531605.2:c.*949C>G	ENSP00000503752.1:n.*949C>G
ENST00000619430.2:c.969C>G	ENSP00000478572.2:p.Phe323Leu
ENST00000676670.1:c.1173C>G	ENSP00000504807.1:p.Phe391Leu
ENST00000676741.1:n.2255C>G
ENST00000677624.1:c.*593C>G	ENSP00000503979.1:n.*593C>G
ENST00000677625.1:c.1119C>G	ENSP00000502857.1:p.Phe373Leu
ENST00000677856.1:n.1426C>G
ENST00000677915.1:c.*70C>G	ENSP00000503118.1:n.*70C>G
ENST00000678533.1:c.*727C>G	ENSP00000503873.1:n.*727C>G
ENST00000678592.1:c.*113C>G	ENSP00000504424.1:n.*113C>G
ENST00000278407.8:c.1173C>G	ENSP00000278407.4:p.Phe391Leu
ENST00000340687.10:c.1062C>G	ENSP00000341861.6:p.Phe354Leu
ENST00000378323.8:c.1188C>G	ENSP00000367574.4:p.Phe396Leu
ENST00000378324.6:c.1017C>G	ENSP00000367575.2:p.Phe339Leu
ENST00000403558.1:c.1302C>G	ENSP00000384420.1:p.Phe434Leu
ENST00000528996.1:c.374C>G	ENSP00000431226.1:n.374C>G
ENST00000530113.1:n.630C>G
ENST00000531133.5:c.674C>G	ENSP00000435431.1:n.674C>G
ENST00000531797.5:c.*198C>G	ENSP00000432554.1:n.*198C>G
ENST00000619430.1:c.349-45C>G	ENSP00000478572.1:n.349-45C>G
NM_000062.2:c.1173C>G , LRG_105t1:c.1173C>G	NP_000053.2:p.Phe391Leu
NM_001032295.1:c.1173C>G	NP_001027466.1:p.Phe391Leu
NM_000062.3:c.1173C>G MANE Select	NP_000053.2:p.Phe391Leu
NM_001032295.2:c.1173C>G	NP_001027466.1:p.Phe391Leu