Canonical Allele Identifier: CA1975539392

Gene: SERPING1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614608C= , CM000673.2:g.57614608C=	GRCh38
NC_000011.9:g.57382081C= , CM000673.1:g.57382081C=	GRCh37
NC_000011.8:g.57138657C=	NCBI36
NG_009625.1:g.22055C= , LRG_105:g.22055C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.*27C= MANE Select	ENSP00000278407.4:n.*27C=
ENST00000528996.2:c.*427C=	ENSP00000431226.2:n.*427C=
ENST00000531605.2:c.*1306C=	ENSP00000503752.1:n.*1306C=
ENST00000619430.2:c.*27C=	ENSP00000478572.2:n.*27C=
ENST00000676670.1:c.*15+12C=	ENSP00000504807.1:n.*15+12C=
ENST00000676741.1:n.2612C=
ENST00000677624.1:c.*950C=	ENSP00000503979.1:n.*950C=
ENST00000677625.1:c.*27C=	ENSP00000502857.1:n.*27C=
ENST00000677856.1:n.1783C=
ENST00000677915.1:c.*427C=	ENSP00000503118.1:n.*427C=
ENST00000678533.1:c.*1072+12C=	ENSP00000503873.1:n.*1072+12C=
ENST00000678592.1:c.*470C=	ENSP00000504424.1:n.*470C=
ENST00000278407.8:c.*27C=	ENSP00000278407.4:n.*27C=
ENST00000340687.10:c.*27C=	ENSP00000341861.6:n.*27C=
ENST00000378323.8:c.*27C=	ENSP00000367574.4:n.*27C=
ENST00000378324.6:c.*27C=	ENSP00000367575.2:n.*27C=
ENST00000403558.1:c.*27C=	ENSP00000384420.1:n.*27C=
ENST00000528996.1:c.731C=	ENSP00000431226.1:n.731C=
ENST00000531797.5:c.*555C=	ENSP00000432554.1:n.*555C=
NM_000062.2:c.*27C= , LRG_105t1:c.*27C=	NP_000053.2:n.*27C=
NM_001032295.1:c.*27C=	NP_001027466.1:n.*27C=
NM_000062.3:c.*27C= MANE Select	NP_000053.2:n.*27C=
NM_001032295.2:c.*27C=	NP_001027466.1:n.*27C=