Canonical Allele Identifier: CA380690274

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381827A>G (hg19) ; chr11:g.57614354A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614354A>G , CM000673.2:g.57614354A>G	GRCh38
NC_000011.9:g.57381827A>G , CM000673.1:g.57381827A>G	GRCh37
NC_000011.8:g.57138403A>G	NCBI36
NG_009625.1:g.21801A>G , LRG_105:g.21801A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1276A>G MANE Select	ENSP00000278407.4:p.Asn426Asp
ENST00000528996.2:c.*173A>G	ENSP00000431226.2:n.*173A>G
ENST00000531605.2:c.*1052A>G	ENSP00000503752.1:n.*1052A>G
ENST00000619430.2:c.1072A>G	ENSP00000478572.2:p.Asn358Asp
ENST00000676670.1:c.1276A>G	ENSP00000504807.1:p.Asn426Asp
ENST00000676741.1:n.2358A>G
ENST00000677624.1:c.*696A>G	ENSP00000503979.1:n.*696A>G
ENST00000677625.1:c.1222A>G	ENSP00000502857.1:p.Asn408Asp
ENST00000677856.1:n.1529A>G
ENST00000677915.1:c.*173A>G	ENSP00000503118.1:n.*173A>G
ENST00000678533.1:c.*830A>G	ENSP00000503873.1:n.*830A>G
ENST00000678592.1:c.*216A>G	ENSP00000504424.1:n.*216A>G
ENST00000278407.8:c.1276A>G	ENSP00000278407.4:p.Asn426Asp
ENST00000340687.10:c.1165A>G	ENSP00000341861.6:p.Asn389Asp
ENST00000378323.8:c.1291A>G	ENSP00000367574.4:p.Asn431Asp
ENST00000378324.6:c.1120A>G	ENSP00000367575.2:p.Asn374Asp
ENST00000403558.1:c.1405A>G	ENSP00000384420.1:p.Asn469Asp
ENST00000528996.1:c.477A>G	ENSP00000431226.1:n.477A>G
ENST00000530113.1:n.733A>G
ENST00000531133.5:c.777A>G	ENSP00000435431.1:n.777A>G
ENST00000531797.5:c.*301A>G	ENSP00000432554.1:n.*301A>G
ENST00000619430.1:c.407A>G	ENSP00000478572.1:n.407A>G
NM_000062.2:c.1276A>G , LRG_105t1:c.1276A>G	NP_000053.2:p.Asn426Asp
NM_001032295.1:c.1276A>G	NP_001027466.1:p.Asn426Asp
NM_000062.3:c.1276A>G MANE Select	NP_000053.2:p.Asn426Asp
NM_001032295.2:c.1276A>G	NP_001027466.1:p.Asn426Asp