Canonical Allele Identifier: CA380690127

Gene: SERPING1

Linked Data

• gnomAD v4: 11-57614332-C-A
• MyVariant Identifiers: chr11:g.57381805C>A (hg19) ; chr11:g.57614332C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614332C>A , CM000673.2:g.57614332C>A	GRCh38
NC_000011.9:g.57381805C>A , CM000673.1:g.57381805C>A	GRCh37
NC_000011.8:g.57138381C>A	NCBI36
NG_009625.1:g.21779C>A , LRG_105:g.21779C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1254C>A MANE Select	ENSP00000278407.4:p.Phe418Leu
ENST00000528996.2:c.*151C>A	ENSP00000431226.2:n.*151C>A
ENST00000531605.2:c.*1030C>A	ENSP00000503752.1:n.*1030C>A
ENST00000619430.2:c.1050C>A	ENSP00000478572.2:p.Phe350Leu
ENST00000676670.1:c.1254C>A	ENSP00000504807.1:p.Phe418Leu
ENST00000676741.1:n.2336C>A
ENST00000677624.1:c.*674C>A	ENSP00000503979.1:n.*674C>A
ENST00000677625.1:c.1200C>A	ENSP00000502857.1:p.Phe400Leu
ENST00000677856.1:n.1507C>A
ENST00000677915.1:c.*151C>A	ENSP00000503118.1:n.*151C>A
ENST00000678533.1:c.*808C>A	ENSP00000503873.1:n.*808C>A
ENST00000678592.1:c.*194C>A	ENSP00000504424.1:n.*194C>A
ENST00000278407.8:c.1254C>A	ENSP00000278407.4:p.Phe418Leu
ENST00000340687.10:c.1143C>A	ENSP00000341861.6:p.Phe381Leu
ENST00000378323.8:c.1269C>A	ENSP00000367574.4:p.Phe423Leu
ENST00000378324.6:c.1098C>A	ENSP00000367575.2:p.Phe366Leu
ENST00000403558.1:c.1383C>A	ENSP00000384420.1:p.Phe461Leu
ENST00000528996.1:c.455C>A	ENSP00000431226.1:n.455C>A
ENST00000530113.1:n.711C>A
ENST00000531133.5:c.755C>A	ENSP00000435431.1:n.755C>A
ENST00000531797.5:c.*279C>A	ENSP00000432554.1:n.*279C>A
ENST00000619430.1:c.385C>A	ENSP00000478572.1:p.Leu129Ile
NM_000062.2:c.1254C>A , LRG_105t1:c.1254C>A	NP_000053.2:p.Phe418Leu
NM_001032295.1:c.1254C>A	NP_001027466.1:p.Phe418Leu
NM_000062.3:c.1254C>A MANE Select	NP_000053.2:p.Phe418Leu
NM_001032295.2:c.1254C>A	NP_001027466.1:p.Phe418Leu