Canonical Allele Identifier: CA1975539523

Gene: SERPING1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614720G= , CM000673.2:g.57614720G=	GRCh38
NC_000011.9:g.57382193G= , CM000673.1:g.57382193G=	GRCh37
NC_000011.8:g.57138769G=	NCBI36
NG_009625.1:g.22167G= , LRG_105:g.22167G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.*139G= MANE Select	ENSP00000278407.4:n.*139G=
ENST00000528996.2:c.*539G=	ENSP00000431226.2:n.*539G=
ENST00000531605.2:c.*1418G=	ENSP00000503752.1:n.*1418G=
ENST00000619430.2:c.*139G=	ENSP00000478572.2:n.*139G=
ENST00000676670.1:c.*15+124G=	ENSP00000504807.1:n.*15+124G=
ENST00000676741.1:n.2724G=
ENST00000677624.1:c.*1062G=	ENSP00000503979.1:n.*1062G=
ENST00000677625.1:c.*139G=	ENSP00000502857.1:n.*139G=
ENST00000677856.1:n.1895G=
ENST00000677915.1:c.*539G=	ENSP00000503118.1:n.*539G=
ENST00000678533.1:c.*1072+124G=	ENSP00000503873.1:n.*1072+124G=
ENST00000678592.1:c.*582G=	ENSP00000504424.1:n.*582G=
ENST00000278407.8:c.*139G=	ENSP00000278407.4:n.*139G=
ENST00000340687.10:c.*139G=	ENSP00000341861.6:n.*139G=
ENST00000378323.8:c.*139G=	ENSP00000367574.4:n.*139G=
ENST00000378324.6:c.*139G=	ENSP00000367575.2:n.*139G=
ENST00000403558.1:c.*139G=	ENSP00000384420.1:n.*139G=
ENST00000528996.1:c.843G=	ENSP00000431226.1:n.843G=
ENST00000531797.5:c.*667G=	ENSP00000432554.1:n.*667G=
NM_000062.2:c.*139G= , LRG_105t1:c.*139G=	NP_000053.2:n.*139G=
NM_001032295.1:c.*139G=	NP_001027466.1:n.*139G=
NM_000062.3:c.*139G= MANE Select	NP_000053.2:n.*139G=
NM_001032295.2:c.*139G=	NP_001027466.1:n.*139G=