Canonical Allele Identifier: CA380702436

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57379220A>T (hg19) ; chr11:g.57611747A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611747A>T , CM000673.2:g.57611747A>T	GRCh38
NC_000011.9:g.57379220A>T , CM000673.1:g.57379220A>T	GRCh37
NC_000011.8:g.57135796A>T	NCBI36
NG_009625.1:g.19194A>T , LRG_105:g.19194A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1060A>T MANE Select	ENSP00000278407.4:p.Ser354Cys
ENST00000528996.2:c.80A>T	ENSP00000431226.2:p.Glu27Val
ENST00000531605.2:c.*836A>T	ENSP00000503752.1:n.*836A>T
ENST00000619430.2:c.856A>T	ENSP00000478572.2:p.Ser286Cys
ENST00000676670.1:c.1060A>T	ENSP00000504807.1:p.Ser354Cys
ENST00000676741.1:n.2142A>T
ENST00000677624.1:c.*480A>T	ENSP00000503979.1:n.*480A>T
ENST00000677625.1:c.1030-24A>T	ENSP00000502857.1:n.1030-24A>T
ENST00000677856.1:n.1313A>T
ENST00000677915.1:c.716A>T	ENSP00000503118.1:p.Glu239Val
ENST00000678533.1:c.*614A>T	ENSP00000503873.1:n.*614A>T
ENST00000678592.1:c.1149A>T	ENSP00000504424.1:p.Ter383Cys
ENST00000278407.8:c.1060A>T	ENSP00000278407.4:p.Ser354Cys
ENST00000340687.10:c.1030-81A>T	ENSP00000341861.6:n.1030-81A>T
ENST00000378323.8:c.1075A>T	ENSP00000367574.4:p.Ser359Cys
ENST00000378324.6:c.904A>T	ENSP00000367575.2:p.Ser302Cys
ENST00000403558.1:c.1189A>T	ENSP00000384420.1:p.Ser397Cys
ENST00000528996.1:c.261A>T	ENSP00000431226.1:p.Ter87Cys
ENST00000530113.1:n.517A>T
ENST00000531133.5:c.561A>T	ENSP00000435431.1:n.561A>T
ENST00000531797.5:c.*85A>T	ENSP00000432554.1:n.*85A>T
ENST00000619430.1:c.349-158A>T	ENSP00000478572.1:n.349-158A>T
NM_000062.2:c.1060A>T , LRG_105t1:c.1060A>T	NP_000053.2:p.Ser354Cys
NM_001032295.1:c.1060A>T	NP_001027466.1:p.Ser354Cys
NM_000062.3:c.1060A>T MANE Select	NP_000053.2:p.Ser354Cys
NM_001032295.2:c.1060A>T	NP_001027466.1:p.Ser354Cys