Canonical Allele Identifier: CA380703146

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57379329A>T (hg19) ; chr11:g.57611856A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611856A>T , CM000673.2:g.57611856A>T	GRCh38
NC_000011.9:g.57379329A>T , CM000673.1:g.57379329A>T	GRCh37
NC_000011.8:g.57135905A>T	NCBI36
NG_009625.1:g.19303A>T , LRG_105:g.19303A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.1169A>T MANE Select	ENSP00000278407.4:p.Lys390Met
ENST00000528996.2:c.*66A>T	ENSP00000431226.2:n.*66A>T
ENST00000531605.2:c.*945A>T	ENSP00000503752.1:n.*945A>T
ENST00000619430.2:c.965A>T	ENSP00000478572.2:p.Lys322Met
ENST00000676670.1:c.1169A>T	ENSP00000504807.1:p.Lys390Met
ENST00000676741.1:n.2251A>T
ENST00000677624.1:c.*589A>T	ENSP00000503979.1:n.*589A>T
ENST00000677625.1:c.1115A>T	ENSP00000502857.1:p.Lys372Met
ENST00000677856.1:n.1422A>T
ENST00000677915.1:c.*66A>T	ENSP00000503118.1:n.*66A>T
ENST00000678533.1:c.*723A>T	ENSP00000503873.1:n.*723A>T
ENST00000678592.1:c.*109A>T	ENSP00000504424.1:n.*109A>T
ENST00000278407.8:c.1169A>T	ENSP00000278407.4:p.Lys390Met
ENST00000340687.10:c.1058A>T	ENSP00000341861.6:p.Lys353Met
ENST00000378323.8:c.1184A>T	ENSP00000367574.4:p.Lys395Met
ENST00000378324.6:c.1013A>T	ENSP00000367575.2:p.Lys338Met
ENST00000403558.1:c.1298A>T	ENSP00000384420.1:p.Lys433Met
ENST00000528996.1:c.370A>T	ENSP00000431226.1:n.370A>T
ENST00000530113.1:n.626A>T
ENST00000531133.5:c.670A>T	ENSP00000435431.1:n.670A>T
ENST00000531797.5:c.*194A>T	ENSP00000432554.1:n.*194A>T
ENST00000619430.1:c.349-49A>T	ENSP00000478572.1:n.349-49A>T
NM_000062.2:c.1169A>T , LRG_105t1:c.1169A>T	NP_000053.2:p.Lys390Met
NM_001032295.1:c.1169A>T	NP_001027466.1:p.Lys390Met
NM_000062.3:c.1169A>T MANE Select	NP_000053.2:p.Lys390Met
NM_001032295.2:c.1169A>T	NP_001027466.1:p.Lys390Met