Canonical Allele Identifier: CA474567645

Gene: SERPING1

Linked Data

• dbSNP Id: rs574198313
• gnomAD v2: 11-57379234-G-A
• gnomAD v4: 11-57611761-G-A
• MyVariant Identifiers: chr11:g.57379234G>A (hg19) ; chr11:g.57611761G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611761G>A , CM000673.2:g.57611761G>A	GRCh38
NC_000011.9:g.57379234G>A , CM000673.1:g.57379234G>A	GRCh37
NC_000011.8:g.57135810G>A	NCBI36
NG_009625.1:g.19208G>A , LRG_105:g.19208G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.1074G>A MANE Select	ENSP00000278407.4:p.Leu358=
ENST00000528996.2:c.94G>A	ENSP00000431226.2:p.Gly32Ser
ENST00000531605.2:c.*850G>A	ENSP00000503752.1:n.*850G>A
ENST00000619430.2:c.870G>A	ENSP00000478572.2:p.Leu290=
ENST00000676670.1:c.1074G>A	ENSP00000504807.1:p.Leu358=
ENST00000676741.1:n.2156G>A
ENST00000677624.1:c.*494G>A	ENSP00000503979.1:n.*494G>A
ENST00000677625.1:c.1030-10G>A	ENSP00000502857.1:n.1030-10G>A
ENST00000677856.1:n.1327G>A
ENST00000677915.1:c.730G>A	ENSP00000503118.1:p.Gly244Ser
ENST00000678533.1:c.*628G>A	ENSP00000503873.1:n.*628G>A
ENST00000678592.1:c.*14G>A	ENSP00000504424.1:n.*14G>A
ENST00000278407.8:c.1074G>A	ENSP00000278407.4:p.Leu358=
ENST00000340687.10:c.1030-67G>A	ENSP00000341861.6:n.1030-67G>A
ENST00000378323.8:c.1089G>A	ENSP00000367574.4:p.Leu363=
ENST00000378324.6:c.918G>A	ENSP00000367575.2:p.Leu306=
ENST00000403558.1:c.1203G>A	ENSP00000384420.1:p.Leu401=
ENST00000528996.1:c.275G>A	ENSP00000431226.1:n.275G>A
ENST00000530113.1:n.531G>A
ENST00000531133.5:c.575G>A	ENSP00000435431.1:n.575G>A
ENST00000531797.5:c.*99G>A	ENSP00000432554.1:n.*99G>A
ENST00000619430.1:c.349-144G>A	ENSP00000478572.1:n.349-144G>A
NM_000062.2:c.1074G>A , LRG_105t1:c.1074G>A	NP_000053.2:p.Leu358=
NM_001032295.1:c.1074G>A	NP_001027466.1:p.Leu358=
NM_000062.3:c.1074G>A MANE Select	NP_000053.2:p.Leu358=
NM_001032295.2:c.1074G>A	NP_001027466.1:p.Leu358=