Canonical Allele Identifier: CA1975537164

Gene: SERPING1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611885C= , CM000673.2:g.57611885C=	GRCh38
NC_000011.9:g.57379358C= , CM000673.1:g.57379358C=	GRCh37
NC_000011.8:g.57135934C=	NCBI36
NG_009625.1:g.19332C= , LRG_105:g.19332C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000062.3:c.1198C= MANE Select	NP_000053.2:p.Arg400=
ENST00000278407.9:c.1198C= MANE Select	ENSP00000278407.4:p.Arg400=
NM_000062.2:c.1198C= , LRG_105t1:c.1198C=	NP_000053.2:p.Arg400=
NM_001032295.1:c.1198C=	NP_001027466.1:p.Arg400=
NM_001032295.2:c.1198C=	NP_001027466.1:p.Arg400=
ENST00000278407.8:c.1198C=	ENSP00000278407.4:p.Arg400=
ENST00000340687.10:c.1087C=	ENSP00000341861.6:p.Arg363=
ENST00000378323.8:c.1213C=	ENSP00000367574.4:p.Arg405=
ENST00000378324.6:c.1042C=	ENSP00000367575.2:p.Arg348=
ENST00000403558.1:c.1327C=	ENSP00000384420.1:p.Arg443=
ENST00000528996.1:c.399C=	ENSP00000431226.1:n.399C=
ENST00000528996.2:c.*95C=	ENSP00000431226.2:n.*95C=
ENST00000530113.1:n.655C=
ENST00000531133.5:c.699C=	ENSP00000435431.1:n.699C=
ENST00000531605.2:c.*974C=	ENSP00000503752.1:n.*974C=
ENST00000531797.5:c.*223C=	ENSP00000432554.1:n.*223C=
ENST00000619430.1:c.349-20C=	ENSP00000478572.1:n.349-20C=
ENST00000619430.2:c.994C=	ENSP00000478572.2:p.Arg332=
ENST00000676670.1:c.1198C=	ENSP00000504807.1:p.Arg400=
ENST00000676741.1:n.2280C=
ENST00000677624.1:c.*618C=	ENSP00000503979.1:n.*618C=
ENST00000677625.1:c.1144C=	ENSP00000502857.1:p.Arg382=
ENST00000677856.1:n.1451C=
ENST00000677915.1:c.*95C=	ENSP00000503118.1:n.*95C=
ENST00000678533.1:c.*752C=	ENSP00000503873.1:n.*752C=
ENST00000678592.1:c.*138C=	ENSP00000504424.1:n.*138C=