Canonical Allele Identifier: CA380690685

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381916G>C (hg19) ; chr11:g.57614443G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614443G>C , CM000673.2:g.57614443G>C	GRCh38
NC_000011.9:g.57381916G>C , CM000673.1:g.57381916G>C	GRCh37
NC_000011.8:g.57138492G>C	NCBI36
NG_009625.1:g.21890G>C , LRG_105:g.21890G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1365G>C MANE Select	ENSP00000278407.4:p.Glu455Asp
ENST00000528996.2:c.*262G>C	ENSP00000431226.2:n.*262G>C
ENST00000531605.2:c.*1141G>C	ENSP00000503752.1:n.*1141G>C
ENST00000619430.2:c.1161G>C	ENSP00000478572.2:p.Glu387Asp
ENST00000676670.1:c.1365G>C	ENSP00000504807.1:p.Glu455Asp
ENST00000676741.1:n.2447G>C
ENST00000677624.1:c.*785G>C	ENSP00000503979.1:n.*785G>C
ENST00000677625.1:c.1311G>C	ENSP00000502857.1:p.Glu437Asp
ENST00000677856.1:n.1618G>C
ENST00000677915.1:c.*262G>C	ENSP00000503118.1:n.*262G>C
ENST00000678533.1:c.*919G>C	ENSP00000503873.1:n.*919G>C
ENST00000678592.1:c.*305G>C	ENSP00000504424.1:n.*305G>C
ENST00000278407.8:c.1365G>C	ENSP00000278407.4:p.Glu455Asp
ENST00000340687.10:c.1254G>C	ENSP00000341861.6:p.Glu418Asp
ENST00000378323.8:c.1380G>C	ENSP00000367574.4:p.Glu460Asp
ENST00000378324.6:c.1209G>C	ENSP00000367575.2:p.Glu403Asp
ENST00000403558.1:c.1494G>C	ENSP00000384420.1:p.Glu498Asp
ENST00000528996.1:c.566G>C	ENSP00000431226.1:n.566G>C
ENST00000530113.1:n.822G>C
ENST00000531133.5:c.866G>C	ENSP00000435431.1:n.866G>C
ENST00000531797.5:c.*390G>C	ENSP00000432554.1:n.*390G>C
ENST00000619430.1:c.496G>C	ENSP00000478572.1:n.496G>C
NM_000062.2:c.1365G>C , LRG_105t1:c.1365G>C	NP_000053.2:p.Glu455Asp
NM_001032295.1:c.1365G>C	NP_001027466.1:p.Glu455Asp
NM_000062.3:c.1365G>C MANE Select	NP_000053.2:p.Glu455Asp
NM_001032295.2:c.1365G>C	NP_001027466.1:p.Glu455Asp