Canonical Allele Identifier: CA1975537142

Gene: SERPING1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611863G= , CM000673.2:g.57611863G=	GRCh38
NC_000011.9:g.57379336G= , CM000673.1:g.57379336G=	GRCh37
NC_000011.8:g.57135912G=	NCBI36
NG_009625.1:g.19310G= , LRG_105:g.19310G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.1176G= MANE Select	ENSP00000278407.4:p.Gln392=
ENST00000528996.2:c.*73G=	ENSP00000431226.2:n.*73G=
ENST00000531605.2:c.*952G=	ENSP00000503752.1:n.*952G=
ENST00000619430.2:c.972G=	ENSP00000478572.2:p.Gln324=
ENST00000676670.1:c.1176G=	ENSP00000504807.1:p.Gln392=
ENST00000676741.1:n.2258G=
ENST00000677624.1:c.*596G=	ENSP00000503979.1:n.*596G=
ENST00000677625.1:c.1122G=	ENSP00000502857.1:p.Gln374=
ENST00000677856.1:n.1429G=
ENST00000677915.1:c.*73G=	ENSP00000503118.1:n.*73G=
ENST00000678533.1:c.*730G=	ENSP00000503873.1:n.*730G=
ENST00000678592.1:c.*116G=	ENSP00000504424.1:n.*116G=
ENST00000278407.8:c.1176G=	ENSP00000278407.4:p.Gln392=
ENST00000340687.10:c.1065G=	ENSP00000341861.6:p.Gln355=
ENST00000378323.8:c.1191G=	ENSP00000367574.4:p.Gln397=
ENST00000378324.6:c.1020G=	ENSP00000367575.2:p.Gln340=
ENST00000403558.1:c.1305G=	ENSP00000384420.1:p.Gln435=
ENST00000528996.1:c.377G=	ENSP00000431226.1:n.377G=
ENST00000530113.1:n.633G=
ENST00000531133.5:c.677G=	ENSP00000435431.1:n.677G=
ENST00000531797.5:c.*201G=	ENSP00000432554.1:n.*201G=
ENST00000619430.1:c.349-42G=	ENSP00000478572.1:n.349-42G=
NM_000062.2:c.1176G= , LRG_105t1:c.1176G=	NP_000053.2:p.Gln392=
NM_001032295.1:c.1176G=	NP_001027466.1:p.Gln392=
NM_000062.3:c.1176G= MANE Select	NP_000053.2:p.Gln392=
NM_001032295.2:c.1176G=	NP_001027466.1:p.Gln392=