Canonical Allele Identifier: CA474567660

Gene: SERPING1

Linked Data

• gnomAD v4: 11-57611764-A-G
• MyVariant Identifiers: chr11:g.57379237A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611764A>G , CM000673.2:g.57611764A>G	GRCh38
NC_000011.9:g.57379237A>G , CM000673.1:g.57379237A>G	GRCh37
NC_000011.8:g.57135813A>G	NCBI36
NG_009625.1:g.19211A>G , LRG_105:g.19211A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.1077A>G MANE Select	ENSP00000278407.4:p.Val359=
ENST00000528996.2:c.97A>G	ENSP00000431226.2:p.Thr33Ala
ENST00000531605.2:c.*853A>G	ENSP00000503752.1:n.*853A>G
ENST00000619430.2:c.873A>G	ENSP00000478572.2:p.Val291=
ENST00000676670.1:c.1077A>G	ENSP00000504807.1:p.Val359=
ENST00000676741.1:n.2159A>G
ENST00000677624.1:c.*497A>G	ENSP00000503979.1:n.*497A>G
ENST00000677625.1:c.1030-7A>G	ENSP00000502857.1:n.1030-7A>G
ENST00000677856.1:n.1330A>G
ENST00000677915.1:c.733A>G	ENSP00000503118.1:p.Thr245Ala
ENST00000678533.1:c.*631A>G	ENSP00000503873.1:n.*631A>G
ENST00000678592.1:c.*17A>G	ENSP00000504424.1:n.*17A>G
ENST00000278407.8:c.1077A>G	ENSP00000278407.4:p.Val359=
ENST00000340687.10:c.1030-64A>G	ENSP00000341861.6:n.1030-64A>G
ENST00000378323.8:c.1092A>G	ENSP00000367574.4:p.Val364=
ENST00000378324.6:c.921A>G	ENSP00000367575.2:p.Val307=
ENST00000403558.1:c.1206A>G	ENSP00000384420.1:p.Val402=
ENST00000528996.1:c.278A>G	ENSP00000431226.1:n.278A>G
ENST00000530113.1:n.534A>G
ENST00000531133.5:c.578A>G	ENSP00000435431.1:n.578A>G
ENST00000531797.5:c.*102A>G	ENSP00000432554.1:n.*102A>G
ENST00000619430.1:c.349-141A>G	ENSP00000478572.1:n.349-141A>G
NM_000062.2:c.1077A>G , LRG_105t1:c.1077A>G	NP_000053.2:p.Val359=
NM_001032295.1:c.1077A>G	NP_001027466.1:p.Val359=
NM_000062.3:c.1077A>G MANE Select	NP_000053.2:p.Val359=
NM_001032295.2:c.1077A>G	NP_001027466.1:p.Val359=