Canonical Allele Identifier: CA474565942

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57369551T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57602078T>C , CM000673.2:g.57602078T>C	GRCh38
NC_000011.9:g.57369551T>C , CM000673.1:g.57369551T>C	GRCh37
NC_000011.8:g.57126127T>C	NCBI36
NG_009625.1:g.9525T>C , LRG_105:g.9525T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.594T>C MANE Select	ENSP00000278407.4:p.Ser198=
ENST00000528996.2:c.58+3750T>C	ENSP00000431226.2:n.58+3750T>C
ENST00000531605.2:c.95T>C	ENSP00000503752.1:p.Leu32Pro
ENST00000619430.2:c.594T>C	ENSP00000478572.2:p.Ser198=
ENST00000676670.1:c.594T>C	ENSP00000504807.1:p.Ser198=
ENST00000676741.1:n.1676T>C
ENST00000677275.1:n.581T>C
ENST00000677624.1:c.594T>C	ENSP00000503979.1:p.Ser198=
ENST00000677625.1:c.594T>C	ENSP00000502857.1:p.Ser198=
ENST00000677856.1:n.653T>C
ENST00000677915.1:c.594T>C	ENSP00000503118.1:p.Ser198=
ENST00000678533.1:c.95T>C	ENSP00000503873.1:p.Leu32Pro
ENST00000678592.1:c.594T>C	ENSP00000504424.1:p.Ser198=
ENST00000278407.8:c.594T>C	ENSP00000278407.4:p.Ser198=
ENST00000340687.10:c.594T>C	ENSP00000341861.6:p.Ser198=
ENST00000378323.8:c.609T>C	ENSP00000367574.4:p.Ser203=
ENST00000378324.6:c.438T>C	ENSP00000367575.2:p.Ser146=
ENST00000403558.1:c.696T>C	ENSP00000384420.1:p.Ser232=
ENST00000531133.5:c.95T>C	ENSP00000435431.1:p.Leu32Pro
ENST00000531605.1:n.34T>C
ENST00000531797.5:c.95T>C	ENSP00000432554.1:p.Leu32Pro
ENST00000619430.1:c.348+1903T>C	ENSP00000478572.1:n.348+1903T>C
NM_000062.2:c.594T>C , LRG_105t1:c.594T>C	NP_000053.2:p.Ser198=
NM_001032295.1:c.594T>C	NP_001027466.1:p.Ser198=
NM_000062.3:c.594T>C MANE Select	NP_000053.2:p.Ser198=
NM_001032295.2:c.594T>C	NP_001027466.1:p.Ser198=