Canonical Allele Identifier: CA474567928

Gene: SERPING1

Linked Data

• gnomAD v4: 11-57611806-T-C
• MyVariant Identifiers: chr11:g.57379279T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611806T>C , CM000673.2:g.57611806T>C	GRCh38
NC_000011.9:g.57379279T>C , CM000673.1:g.57379279T>C	GRCh37
NC_000011.8:g.57135855T>C	NCBI36
NG_009625.1:g.19253T>C , LRG_105:g.19253T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1119T>C MANE Select	ENSP00000278407.4:p.Ala373=
ENST00000528996.2:c.*16T>C	ENSP00000431226.2:n.*16T>C
ENST00000531605.2:c.*895T>C	ENSP00000503752.1:n.*895T>C
ENST00000619430.2:c.915T>C	ENSP00000478572.2:p.Ala305=
ENST00000676670.1:c.1119T>C	ENSP00000504807.1:p.Ala373=
ENST00000676741.1:n.2201T>C
ENST00000677624.1:c.*539T>C	ENSP00000503979.1:n.*539T>C
ENST00000677625.1:c.1065T>C	ENSP00000502857.1:p.Ala355=
ENST00000677856.1:n.1372T>C
ENST00000677915.1:c.*16T>C	ENSP00000503118.1:n.*16T>C
ENST00000678533.1:c.*673T>C	ENSP00000503873.1:n.*673T>C
ENST00000678592.1:c.*59T>C	ENSP00000504424.1:n.*59T>C
ENST00000278407.8:c.1119T>C	ENSP00000278407.4:p.Ala373=
ENST00000340687.10:c.1030-22T>C	ENSP00000341861.6:n.1030-22T>C
ENST00000378323.8:c.1134T>C	ENSP00000367574.4:p.Ala378=
ENST00000378324.6:c.963T>C	ENSP00000367575.2:p.Ala321=
ENST00000403558.1:c.1248T>C	ENSP00000384420.1:p.Ala416=
ENST00000528996.1:c.320T>C	ENSP00000431226.1:n.320T>C
ENST00000530113.1:n.576T>C
ENST00000531133.5:c.620T>C	ENSP00000435431.1:n.620T>C
ENST00000531797.5:c.*144T>C	ENSP00000432554.1:n.*144T>C
ENST00000619430.1:c.349-99T>C	ENSP00000478572.1:n.349-99T>C
NM_000062.2:c.1119T>C , LRG_105t1:c.1119T>C	NP_000053.2:p.Ala373=
NM_001032295.1:c.1119T>C	NP_001027466.1:p.Ala373=
NM_000062.3:c.1119T>C MANE Select	NP_000053.2:p.Ala373=
NM_001032295.2:c.1119T>C	NP_001027466.1:p.Ala373=