Canonical Allele Identifier: CA1975539197

Gene: SERPING1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614450G= , CM000673.2:g.57614450G=	GRCh38
NC_000011.9:g.57381923G= , CM000673.1:g.57381923G=	GRCh37
NC_000011.8:g.57138499G=	NCBI36
NG_009625.1:g.21897G= , LRG_105:g.21897G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1372G= MANE Select	ENSP00000278407.4:p.Ala458=
ENST00000528996.2:c.*269G=	ENSP00000431226.2:n.*269G=
ENST00000531605.2:c.*1148G=	ENSP00000503752.1:n.*1148G=
ENST00000619430.2:c.1168G=	ENSP00000478572.2:p.Ala390=
ENST00000676670.1:c.1372G=	ENSP00000504807.1:p.Ala458=
ENST00000676741.1:n.2454G=
ENST00000677624.1:c.*792G=	ENSP00000503979.1:n.*792G=
ENST00000677625.1:c.1318G=	ENSP00000502857.1:p.Ala440=
ENST00000677856.1:n.1625G=
ENST00000677915.1:c.*269G=	ENSP00000503118.1:n.*269G=
ENST00000678533.1:c.*926G=	ENSP00000503873.1:n.*926G=
ENST00000678592.1:c.*312G=	ENSP00000504424.1:n.*312G=
ENST00000278407.8:c.1372G=	ENSP00000278407.4:p.Ala458=
ENST00000340687.10:c.1261G=	ENSP00000341861.6:p.Ala421=
ENST00000378323.8:c.1387G=	ENSP00000367574.4:p.Ala463=
ENST00000378324.6:c.1216G=	ENSP00000367575.2:p.Ala406=
ENST00000403558.1:c.1501G=	ENSP00000384420.1:p.Ala501=
ENST00000528996.1:c.573G=	ENSP00000431226.1:n.573G=
ENST00000530113.1:n.829G=
ENST00000531133.5:c.873G=	ENSP00000435431.1:n.873G=
ENST00000531797.5:c.*397G=	ENSP00000432554.1:n.*397G=
ENST00000619430.1:c.503G=	ENSP00000478572.1:n.503G=
NM_000062.2:c.1372G= , LRG_105t1:c.1372G=	NP_000053.2:p.Ala458=
NM_001032295.1:c.1372G=	NP_001027466.1:p.Ala458=
NM_000062.3:c.1372G= MANE Select	NP_000053.2:p.Ala458=
NM_001032295.2:c.1372G=	NP_001027466.1:p.Ala458=