Canonical Allele Identifier: CA1975539286

Gene: SERPING1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614498C= , CM000673.2:g.57614498C=	GRCh38
NC_000011.9:g.57381971C= , CM000673.1:g.57381971C=	GRCh37
NC_000011.8:g.57138547C=	NCBI36
NG_009625.1:g.21945C= , LRG_105:g.21945C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1420C= MANE Select	ENSP00000278407.4:p.Gln474=
ENST00000528996.2:c.*317C=	ENSP00000431226.2:n.*317C=
ENST00000531605.2:c.*1196C=	ENSP00000503752.1:n.*1196C=
ENST00000619430.2:c.1216C=	ENSP00000478572.2:p.Gln406=
ENST00000676670.1:c.1420C=	ENSP00000504807.1:p.Gln474=
ENST00000676741.1:n.2502C=
ENST00000677624.1:c.*840C=	ENSP00000503979.1:n.*840C=
ENST00000677625.1:c.1366C=	ENSP00000502857.1:p.Gln456=
ENST00000677856.1:n.1673C=
ENST00000677915.1:c.*317C=	ENSP00000503118.1:n.*317C=
ENST00000678533.1:c.*974C=	ENSP00000503873.1:n.*974C=
ENST00000678592.1:c.*360C=	ENSP00000504424.1:n.*360C=
ENST00000278407.8:c.1420C=	ENSP00000278407.4:p.Gln474=
ENST00000340687.10:c.1309C=	ENSP00000341861.6:p.Gln437=
ENST00000378323.8:c.1435C=	ENSP00000367574.4:p.Gln479=
ENST00000378324.6:c.1264C=	ENSP00000367575.2:p.Gln422=
ENST00000403558.1:c.1549C=	ENSP00000384420.1:p.Gln517=
ENST00000528996.1:c.621C=	ENSP00000431226.1:n.621C=
ENST00000530113.1:n.877C=
ENST00000531133.5:c.921C=	ENSP00000435431.1:n.921C=
ENST00000531797.5:c.*445C=	ENSP00000432554.1:n.*445C=
ENST00000619430.1:c.551C=	ENSP00000478572.1:n.551C=
NM_000062.2:c.1420C= , LRG_105t1:c.1420C=	NP_000053.2:p.Gln474=
NM_001032295.1:c.1420C=	NP_001027466.1:p.Gln474=
NM_000062.3:c.1420C= MANE Select	NP_000053.2:p.Gln474=
NM_001032295.2:c.1420C=	NP_001027466.1:p.Gln474=