Canonical Allele Identifier: CA380690804

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381978C>G (hg19) ; chr11:g.57614505C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614505C>G , CM000673.2:g.57614505C>G	GRCh38
NC_000011.9:g.57381978C>G , CM000673.1:g.57381978C>G	GRCh37
NC_000011.8:g.57138554C>G	NCBI36
NG_009625.1:g.21952C>G , LRG_105:g.21952C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1427C>G MANE Select	ENSP00000278407.4:p.Pro476Arg
ENST00000528996.2:c.*324C>G	ENSP00000431226.2:n.*324C>G
ENST00000531605.2:c.*1203C>G	ENSP00000503752.1:n.*1203C>G
ENST00000619430.2:c.1223C>G	ENSP00000478572.2:p.Pro408Arg
ENST00000676670.1:c.1427C>G	ENSP00000504807.1:p.Pro476Arg
ENST00000676741.1:n.2509C>G
ENST00000677624.1:c.*847C>G	ENSP00000503979.1:n.*847C>G
ENST00000677625.1:c.1373C>G	ENSP00000502857.1:p.Pro458Arg
ENST00000677856.1:n.1680C>G
ENST00000677915.1:c.*324C>G	ENSP00000503118.1:n.*324C>G
ENST00000678533.1:c.*981C>G	ENSP00000503873.1:n.*981C>G
ENST00000678592.1:c.*367C>G	ENSP00000504424.1:n.*367C>G
ENST00000278407.8:c.1427C>G	ENSP00000278407.4:p.Pro476Arg
ENST00000340687.10:c.1316C>G	ENSP00000341861.6:p.Pro439Arg
ENST00000378323.8:c.1442C>G	ENSP00000367574.4:p.Pro481Arg
ENST00000378324.6:c.1271C>G	ENSP00000367575.2:p.Pro424Arg
ENST00000403558.1:c.1556C>G	ENSP00000384420.1:p.Pro519Arg
ENST00000528996.1:c.628C>G	ENSP00000431226.1:n.628C>G
ENST00000530113.1:n.884C>G
ENST00000531133.5:c.928C>G	ENSP00000435431.1:n.928C>G
ENST00000531797.5:c.*452C>G	ENSP00000432554.1:n.*452C>G
ENST00000619430.1:c.558C>G	ENSP00000478572.1:n.558C>G
NM_000062.2:c.1427C>G , LRG_105t1:c.1427C>G	NP_000053.2:p.Pro476Arg
NM_001032295.1:c.1427C>G	NP_001027466.1:p.Pro476Arg
NM_000062.3:c.1427C>G MANE Select	NP_000053.2:p.Pro476Arg
NM_001032295.2:c.1427C>G	NP_001027466.1:p.Pro476Arg