Canonical Allele Identifier: CA380702526

Gene: SERPING1

Linked Data

• gnomAD v4: 11-57611762-G-A
• MyVariant Identifiers: chr11:g.57379235G>A (hg19) ; chr11:g.57611762G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611762G>A , CM000673.2:g.57611762G>A	GRCh38
NC_000011.9:g.57379235G>A , CM000673.1:g.57379235G>A	GRCh37
NC_000011.8:g.57135811G>A	NCBI36
NG_009625.1:g.19209G>A , LRG_105:g.19209G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.1075G>A MANE Select	ENSP00000278407.4:p.Val359Ile
ENST00000528996.2:c.95G>A	ENSP00000431226.2:p.Gly32Asp
ENST00000531605.2:c.*851G>A	ENSP00000503752.1:n.*851G>A
ENST00000619430.2:c.871G>A	ENSP00000478572.2:p.Val291Ile
ENST00000676670.1:c.1075G>A	ENSP00000504807.1:p.Val359Ile
ENST00000676741.1:n.2157G>A
ENST00000677624.1:c.*495G>A	ENSP00000503979.1:n.*495G>A
ENST00000677625.1:c.1030-9G>A	ENSP00000502857.1:n.1030-9G>A
ENST00000677856.1:n.1328G>A
ENST00000677915.1:c.731G>A	ENSP00000503118.1:p.Gly244Asp
ENST00000678533.1:c.*629G>A	ENSP00000503873.1:n.*629G>A
ENST00000678592.1:c.*15G>A	ENSP00000504424.1:n.*15G>A
ENST00000278407.8:c.1075G>A	ENSP00000278407.4:p.Val359Ile
ENST00000340687.10:c.1030-66G>A	ENSP00000341861.6:n.1030-66G>A
ENST00000378323.8:c.1090G>A	ENSP00000367574.4:p.Val364Ile
ENST00000378324.6:c.919G>A	ENSP00000367575.2:p.Val307Ile
ENST00000403558.1:c.1204G>A	ENSP00000384420.1:p.Val402Ile
ENST00000528996.1:c.276G>A	ENSP00000431226.1:n.276G>A
ENST00000530113.1:n.532G>A
ENST00000531133.5:c.576G>A	ENSP00000435431.1:n.576G>A
ENST00000531797.5:c.*100G>A	ENSP00000432554.1:n.*100G>A
ENST00000619430.1:c.349-143G>A	ENSP00000478572.1:n.349-143G>A
NM_000062.2:c.1075G>A , LRG_105t1:c.1075G>A	NP_000053.2:p.Val359Ile
NM_001032295.1:c.1075G>A	NP_001027466.1:p.Val359Ile
NM_000062.3:c.1075G>A MANE Select	NP_000053.2:p.Val359Ile
NM_001032295.2:c.1075G>A	NP_001027466.1:p.Val359Ile