Canonical Allele Identifier: CA380690745

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381951C>A (hg19) ; chr11:g.57614478C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614478C>A , CM000673.2:g.57614478C>A	GRCh38
NC_000011.9:g.57381951C>A , CM000673.1:g.57381951C>A	GRCh37
NC_000011.8:g.57138527C>A	NCBI36
NG_009625.1:g.21925C>A , LRG_105:g.21925C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1400C>A MANE Select	ENSP00000278407.4:p.Thr467Asn
ENST00000528996.2:c.*297C>A	ENSP00000431226.2:n.*297C>A
ENST00000531605.2:c.*1176C>A	ENSP00000503752.1:n.*1176C>A
ENST00000619430.2:c.1196C>A	ENSP00000478572.2:p.Thr399Asn
ENST00000676670.1:c.1400C>A	ENSP00000504807.1:p.Thr467Asn
ENST00000676741.1:n.2482C>A
ENST00000677624.1:c.*820C>A	ENSP00000503979.1:n.*820C>A
ENST00000677625.1:c.1346C>A	ENSP00000502857.1:p.Thr449Asn
ENST00000677856.1:n.1653C>A
ENST00000677915.1:c.*297C>A	ENSP00000503118.1:n.*297C>A
ENST00000678533.1:c.*954C>A	ENSP00000503873.1:n.*954C>A
ENST00000678592.1:c.*340C>A	ENSP00000504424.1:n.*340C>A
ENST00000278407.8:c.1400C>A	ENSP00000278407.4:p.Thr467Asn
ENST00000340687.10:c.1289C>A	ENSP00000341861.6:p.Thr430Asn
ENST00000378323.8:c.1415C>A	ENSP00000367574.4:p.Thr472Asn
ENST00000378324.6:c.1244C>A	ENSP00000367575.2:p.Thr415Asn
ENST00000403558.1:c.1529C>A	ENSP00000384420.1:p.Thr510Asn
ENST00000528996.1:c.601C>A	ENSP00000431226.1:n.601C>A
ENST00000530113.1:n.857C>A
ENST00000531133.5:c.901C>A	ENSP00000435431.1:n.901C>A
ENST00000531797.5:c.*425C>A	ENSP00000432554.1:n.*425C>A
ENST00000619430.1:c.531C>A	ENSP00000478572.1:n.531C>A
NM_000062.2:c.1400C>A , LRG_105t1:c.1400C>A	NP_000053.2:p.Thr467Asn
NM_001032295.1:c.1400C>A	NP_001027466.1:p.Thr467Asn
NM_000062.3:c.1400C>A MANE Select	NP_000053.2:p.Thr467Asn
NM_001032295.2:c.1400C>A	NP_001027466.1:p.Thr467Asn