Canonical Allele Identifier: CA1975539372

Gene: SERPING1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614577C= , CM000673.2:g.57614577C=	GRCh38
NC_000011.9:g.57382050C= , CM000673.1:g.57382050C=	GRCh37
NC_000011.8:g.57138626C=	NCBI36
NG_009625.1:g.22024C= , LRG_105:g.22024C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1499C= MANE Select	ENSP00000278407.4:p.Ala500=
ENST00000528996.2:c.*396C=	ENSP00000431226.2:n.*396C=
ENST00000531605.2:c.*1275C=	ENSP00000503752.1:n.*1275C=
ENST00000619430.2:c.1295C=	ENSP00000478572.2:p.Ala432=
ENST00000676670.1:c.1499C=	ENSP00000504807.1:p.Ala500=
ENST00000676741.1:n.2581C=
ENST00000677624.1:c.*919C=	ENSP00000503979.1:n.*919C=
ENST00000677625.1:c.1445C=	ENSP00000502857.1:p.Ala482=
ENST00000677856.1:n.1752C=
ENST00000677915.1:c.*396C=	ENSP00000503118.1:n.*396C=
ENST00000678533.1:c.*1053C=	ENSP00000503873.1:n.*1053C=
ENST00000678592.1:c.*439C=	ENSP00000504424.1:n.*439C=
ENST00000278407.8:c.1499C=	ENSP00000278407.4:p.Ala500=
ENST00000340687.10:c.1388C=	ENSP00000341861.6:p.Ala463=
ENST00000378323.8:c.1514C=	ENSP00000367574.4:p.Ala505=
ENST00000378324.6:c.1343C=	ENSP00000367575.2:p.Ala448=
ENST00000403558.1:c.1628C=	ENSP00000384420.1:p.Ala543=
ENST00000528996.1:c.700C=	ENSP00000431226.1:n.700C=
ENST00000531133.5:c.1000C=	ENSP00000435431.1:n.1000C=
ENST00000531797.5:c.*524C=	ENSP00000432554.1:n.*524C=
ENST00000619430.1:c.630C=	ENSP00000478572.1:n.630C=
NM_000062.2:c.1499C= , LRG_105t1:c.1499C=	NP_000053.2:p.Ala500=
NM_001032295.1:c.1499C=	NP_001027466.1:p.Ala500=
NM_000062.3:c.1499C= MANE Select	NP_000053.2:p.Ala500=
NM_001032295.2:c.1499C=	NP_001027466.1:p.Ala500=