Canonical Allele Identifier: CA1975536195

Gene: SERPING1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57610920T= , CM000673.2:g.57610920T=	GRCh38
NC_000011.9:g.57378393T= , CM000673.1:g.57378393T=	GRCh37
NC_000011.8:g.57134969T=	NCBI36
NG_009625.1:g.18367T= , LRG_105:g.18367T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1030-797T= MANE Select	ENSP00000278407.4:n.1030-797T=
ENST00000528996.2:c.59-806T=	ENSP00000431226.2:n.59-806T=
ENST00000531605.2:c.*806-797T=	ENSP00000503752.1:n.*806-797T=
ENST00000619430.2:c.826-797T=	ENSP00000478572.2:n.826-797T=
ENST00000676670.1:c.1030-797T=	ENSP00000504807.1:n.1030-797T=
ENST00000676741.1:n.2112-797T=
ENST00000677624.1:c.*450-797T=	ENSP00000503979.1:n.*450-797T=
ENST00000677625.1:c.1030-851T=	ENSP00000502857.1:n.1030-851T=
ENST00000677856.1:n.1283-797T=
ENST00000677915.1:c.686-797T=	ENSP00000503118.1:n.686-797T=
ENST00000678533.1:c.*584-797T=	ENSP00000503873.1:n.*584-797T=
ENST00000678592.1:c.1119-797T=	ENSP00000504424.1:n.1119-797T=
ENST00000278407.8:c.1030-797T=	ENSP00000278407.4:n.1030-797T=
ENST00000340687.10:c.1030-908T=	ENSP00000341861.6:n.1030-908T=
ENST00000378323.8:c.1045-797T=	ENSP00000367574.4:n.1045-797T=
ENST00000378324.6:c.874-797T=	ENSP00000367575.2:n.874-797T=
ENST00000403558.1:c.1159-797T=	ENSP00000384420.1:n.1159-797T=
ENST00000528996.1:c.231-797T=	ENSP00000431226.1:n.231-797T=
ENST00000531133.5:c.531-797T=	ENSP00000435431.1:n.531-797T=
ENST00000531797.5:c.*55-797T=	ENSP00000432554.1:n.*55-797T=
ENST00000619430.1:c.349-985T=	ENSP00000478572.1:n.349-985T=
NM_000062.2:c.1030-797T= , LRG_105t1:c.1030-797T=	NP_000053.2:n.1030-797T=
NM_001032295.1:c.1030-797T=	NP_001027466.1:n.1030-797T=
NM_000062.3:c.1030-797T= MANE Select	NP_000053.2:n.1030-797T=
NM_001032295.2:c.1030-797T=	NP_001027466.1:n.1030-797T=