Canonical Allele Identifier: CA380690865

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57382004C>A (hg19) ; chr11:g.57614531C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614531C>A , CM000673.2:g.57614531C>A	GRCh38
NC_000011.9:g.57382004C>A , CM000673.1:g.57382004C>A	GRCh37
NC_000011.8:g.57138580C>A	NCBI36
NG_009625.1:g.21978C>A , LRG_105:g.21978C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1453C>A MANE Select	ENSP00000278407.4:p.Gln485Lys
ENST00000528996.2:c.*350C>A	ENSP00000431226.2:n.*350C>A
ENST00000531605.2:c.*1229C>A	ENSP00000503752.1:n.*1229C>A
ENST00000619430.2:c.1249C>A	ENSP00000478572.2:p.Gln417Lys
ENST00000676670.1:c.1453C>A	ENSP00000504807.1:p.Gln485Lys
ENST00000676741.1:n.2535C>A
ENST00000677624.1:c.*873C>A	ENSP00000503979.1:n.*873C>A
ENST00000677625.1:c.1399C>A	ENSP00000502857.1:p.Gln467Lys
ENST00000677856.1:n.1706C>A
ENST00000677915.1:c.*350C>A	ENSP00000503118.1:n.*350C>A
ENST00000678533.1:c.*1007C>A	ENSP00000503873.1:n.*1007C>A
ENST00000678592.1:c.*393C>A	ENSP00000504424.1:n.*393C>A
ENST00000278407.8:c.1453C>A	ENSP00000278407.4:p.Gln485Lys
ENST00000340687.10:c.1342C>A	ENSP00000341861.6:p.Gln448Lys
ENST00000378323.8:c.1468C>A	ENSP00000367574.4:p.Gln490Lys
ENST00000378324.6:c.1297C>A	ENSP00000367575.2:p.Gln433Lys
ENST00000403558.1:c.1582C>A	ENSP00000384420.1:p.Gln528Lys
ENST00000528996.1:c.654C>A	ENSP00000431226.1:n.654C>A
ENST00000531133.5:c.954C>A	ENSP00000435431.1:n.954C>A
ENST00000531797.5:c.*478C>A	ENSP00000432554.1:n.*478C>A
ENST00000619430.1:c.584C>A	ENSP00000478572.1:n.584C>A
NM_000062.2:c.1453C>A , LRG_105t1:c.1453C>A	NP_000053.2:p.Gln485Lys
NM_001032295.1:c.1453C>A	NP_001027466.1:p.Gln485Lys
NM_000062.3:c.1453C>A MANE Select	NP_000053.2:p.Gln485Lys
NM_001032295.2:c.1453C>A	NP_001027466.1:p.Gln485Lys