Canonical Allele Identifier: CA1975539035

Gene: SERPING1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614350C= , CM000673.2:g.57614350C=	GRCh38
NC_000011.9:g.57381823C= , CM000673.1:g.57381823C=	GRCh37
NC_000011.8:g.57138399C=	NCBI36
NG_009625.1:g.21797C= , LRG_105:g.21797C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1272C= MANE Select	ENSP00000278407.4:p.Asp424=
ENST00000528996.2:c.*169C=	ENSP00000431226.2:n.*169C=
ENST00000531605.2:c.*1048C=	ENSP00000503752.1:n.*1048C=
ENST00000619430.2:c.1068C=	ENSP00000478572.2:p.Asp356=
ENST00000676670.1:c.1272C=	ENSP00000504807.1:p.Asp424=
ENST00000676741.1:n.2354C=
ENST00000677624.1:c.*692C=	ENSP00000503979.1:n.*692C=
ENST00000677625.1:c.1218C=	ENSP00000502857.1:p.Asp406=
ENST00000677856.1:n.1525C=
ENST00000677915.1:c.*169C=	ENSP00000503118.1:n.*169C=
ENST00000678533.1:c.*826C=	ENSP00000503873.1:n.*826C=
ENST00000678592.1:c.*212C=	ENSP00000504424.1:n.*212C=
ENST00000278407.8:c.1272C=	ENSP00000278407.4:p.Asp424=
ENST00000340687.10:c.1161C=	ENSP00000341861.6:p.Asp387=
ENST00000378323.8:c.1287C=	ENSP00000367574.4:p.Asp429=
ENST00000378324.6:c.1116C=	ENSP00000367575.2:p.Asp372=
ENST00000403558.1:c.1401C=	ENSP00000384420.1:p.Asp467=
ENST00000528996.1:c.473C=	ENSP00000431226.1:n.473C=
ENST00000530113.1:n.729C=
ENST00000531133.5:c.773C=	ENSP00000435431.1:n.773C=
ENST00000531797.5:c.*297C=	ENSP00000432554.1:n.*297C=
ENST00000619430.1:c.403C=	ENSP00000478572.1:n.403C=
NM_000062.2:c.1272C= , LRG_105t1:c.1272C=	NP_000053.2:p.Asp424=
NM_001032295.1:c.1272C=	NP_001027466.1:p.Asp424=
NM_000062.3:c.1272C= MANE Select	NP_000053.2:p.Asp424=
NM_001032295.2:c.1272C=	NP_001027466.1:p.Asp424=