Canonical Allele Identifier: CA380703467

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57379384T>A (hg19) ; chr11:g.57611911T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611911T>A , CM000673.2:g.57611911T>A	GRCh38
NC_000011.9:g.57379384T>A , CM000673.1:g.57379384T>A	GRCh37
NC_000011.8:g.57135960T>A	NCBI36
NG_009625.1:g.19358T>A , LRG_105:g.19358T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1224T>A MANE Select	ENSP00000278407.4:p.Asp408Glu
ENST00000528996.2:c.*121T>A	ENSP00000431226.2:n.*121T>A
ENST00000531605.2:c.*1000T>A	ENSP00000503752.1:n.*1000T>A
ENST00000619430.2:c.1020T>A	ENSP00000478572.2:p.Asp340Glu
ENST00000676670.1:c.1224T>A	ENSP00000504807.1:p.Asp408Glu
ENST00000676741.1:n.2306T>A
ENST00000677624.1:c.*644T>A	ENSP00000503979.1:n.*644T>A
ENST00000677625.1:c.1170T>A	ENSP00000502857.1:p.Asp390Glu
ENST00000677856.1:n.1477T>A
ENST00000677915.1:c.*121T>A	ENSP00000503118.1:n.*121T>A
ENST00000678533.1:c.*778T>A	ENSP00000503873.1:n.*778T>A
ENST00000678592.1:c.*164T>A	ENSP00000504424.1:n.*164T>A
ENST00000278407.8:c.1224T>A	ENSP00000278407.4:p.Asp408Glu
ENST00000340687.10:c.1113T>A	ENSP00000341861.6:p.Asp371Glu
ENST00000378323.8:c.1239T>A	ENSP00000367574.4:p.Asp413Glu
ENST00000378324.6:c.1068T>A	ENSP00000367575.2:p.Asp356Glu
ENST00000403558.1:c.1353T>A	ENSP00000384420.1:p.Asp451Glu
ENST00000528996.1:c.425T>A	ENSP00000431226.1:n.425T>A
ENST00000530113.1:n.681T>A
ENST00000531133.5:c.725T>A	ENSP00000435431.1:n.725T>A
ENST00000531797.5:c.*249T>A	ENSP00000432554.1:n.*249T>A
ENST00000619430.1:c.355T>A	ENSP00000478572.1:p.Tyr119Asn
NM_000062.2:c.1224T>A , LRG_105t1:c.1224T>A	NP_000053.2:p.Asp408Glu
NM_001032295.1:c.1224T>A	NP_001027466.1:p.Asp408Glu
NM_000062.3:c.1224T>A MANE Select	NP_000053.2:p.Asp408Glu
NM_001032295.2:c.1224T>A	NP_001027466.1:p.Asp408Glu