Canonical Allele Identifier: CA1975539413

Gene: SERPING1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614626A= , CM000673.2:g.57614626A=	GRCh38
NC_000011.9:g.57382099A= , CM000673.1:g.57382099A=	GRCh37
NC_000011.8:g.57138675A=	NCBI36
NG_009625.1:g.22073A= , LRG_105:g.22073A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.*45A= MANE Select	ENSP00000278407.4:n.*45A=
ENST00000528996.2:c.*445A=	ENSP00000431226.2:n.*445A=
ENST00000531605.2:c.*1324A=	ENSP00000503752.1:n.*1324A=
ENST00000619430.2:c.*45A=	ENSP00000478572.2:n.*45A=
ENST00000676670.1:c.*15+30A=	ENSP00000504807.1:n.*15+30A=
ENST00000676741.1:n.2630A=
ENST00000677624.1:c.*968A=	ENSP00000503979.1:n.*968A=
ENST00000677625.1:c.*45A=	ENSP00000502857.1:n.*45A=
ENST00000677856.1:n.1801A=
ENST00000677915.1:c.*445A=	ENSP00000503118.1:n.*445A=
ENST00000678533.1:c.*1072+30A=	ENSP00000503873.1:n.*1072+30A=
ENST00000678592.1:c.*488A=	ENSP00000504424.1:n.*488A=
ENST00000278407.8:c.*45A=	ENSP00000278407.4:n.*45A=
ENST00000340687.10:c.*45A=	ENSP00000341861.6:n.*45A=
ENST00000378323.8:c.*45A=	ENSP00000367574.4:n.*45A=
ENST00000378324.6:c.*45A=	ENSP00000367575.2:n.*45A=
ENST00000403558.1:c.*45A=	ENSP00000384420.1:n.*45A=
ENST00000528996.1:c.749A=	ENSP00000431226.1:n.749A=
ENST00000531797.5:c.*573A=	ENSP00000432554.1:n.*573A=
NM_000062.2:c.*45A= , LRG_105t1:c.*45A=	NP_000053.2:n.*45A=
NM_001032295.1:c.*45A=	NP_001027466.1:n.*45A=
NM_000062.3:c.*45A= MANE Select	NP_000053.2:n.*45A=
NM_001032295.2:c.*45A=	NP_001027466.1:n.*45A=