Canonical Allele Identifier: CA380690811

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381981T>C (hg19) ; chr11:g.57614508T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614508T>C , CM000673.2:g.57614508T>C	GRCh38
NC_000011.9:g.57381981T>C , CM000673.1:g.57381981T>C	GRCh37
NC_000011.8:g.57138557T>C	NCBI36
NG_009625.1:g.21955T>C , LRG_105:g.21955T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1430T>C MANE Select	ENSP00000278407.4:p.Phe477Ser
ENST00000528996.2:c.*327T>C	ENSP00000431226.2:n.*327T>C
ENST00000531605.2:c.*1206T>C	ENSP00000503752.1:n.*1206T>C
ENST00000619430.2:c.1226T>C	ENSP00000478572.2:p.Phe409Ser
ENST00000676670.1:c.1430T>C	ENSP00000504807.1:p.Phe477Ser
ENST00000676741.1:n.2512T>C
ENST00000677624.1:c.*850T>C	ENSP00000503979.1:n.*850T>C
ENST00000677625.1:c.1376T>C	ENSP00000502857.1:p.Phe459Ser
ENST00000677856.1:n.1683T>C
ENST00000677915.1:c.*327T>C	ENSP00000503118.1:n.*327T>C
ENST00000678533.1:c.*984T>C	ENSP00000503873.1:n.*984T>C
ENST00000678592.1:c.*370T>C	ENSP00000504424.1:n.*370T>C
ENST00000278407.8:c.1430T>C	ENSP00000278407.4:p.Phe477Ser
ENST00000340687.10:c.1319T>C	ENSP00000341861.6:p.Phe440Ser
ENST00000378323.8:c.1445T>C	ENSP00000367574.4:p.Phe482Ser
ENST00000378324.6:c.1274T>C	ENSP00000367575.2:p.Phe425Ser
ENST00000403558.1:c.1559T>C	ENSP00000384420.1:p.Phe520Ser
ENST00000528996.1:c.631T>C	ENSP00000431226.1:n.631T>C
ENST00000530113.1:n.887T>C
ENST00000531133.5:c.931T>C	ENSP00000435431.1:n.931T>C
ENST00000531797.5:c.*455T>C	ENSP00000432554.1:n.*455T>C
ENST00000619430.1:c.561T>C	ENSP00000478572.1:n.561T>C
NM_000062.2:c.1430T>C , LRG_105t1:c.1430T>C	NP_000053.2:p.Phe477Ser
NM_001032295.1:c.1430T>C	NP_001027466.1:p.Phe477Ser
NM_000062.3:c.1430T>C MANE Select	NP_000053.2:p.Phe477Ser
NM_001032295.2:c.1430T>C	NP_001027466.1:p.Phe477Ser