Canonical Allele Identifier: CA380690977

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57382054A>T (hg19) ; chr11:g.57614581A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614581A>T , CM000673.2:g.57614581A>T	GRCh38
NC_000011.9:g.57382054A>T , CM000673.1:g.57382054A>T	GRCh37
NC_000011.8:g.57138630A>T	NCBI36
NG_009625.1:g.22028A>T , LRG_105:g.22028A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1503A>T MANE Select	ENSP00000278407.4:p.Ter501Cys
ENST00000528996.2:c.*400A>T	ENSP00000431226.2:n.*400A>T
ENST00000531605.2:c.*1279A>T	ENSP00000503752.1:n.*1279A>T
ENST00000619430.2:c.1299A>T	ENSP00000478572.2:p.Ter433Cys
ENST00000676670.1:c.1503A>T	ENSP00000504807.1:p.Ter501Cys
ENST00000676741.1:n.2585A>T
ENST00000677624.1:c.*923A>T	ENSP00000503979.1:n.*923A>T
ENST00000677625.1:c.1449A>T	ENSP00000502857.1:p.Ter483Cys
ENST00000677856.1:n.1756A>T
ENST00000677915.1:c.*400A>T	ENSP00000503118.1:n.*400A>T
ENST00000678533.1:c.*1057A>T	ENSP00000503873.1:n.*1057A>T
ENST00000678592.1:c.*443A>T	ENSP00000504424.1:n.*443A>T
ENST00000278407.8:c.1503A>T	ENSP00000278407.4:p.Ter501Cys
ENST00000340687.10:c.1392A>T	ENSP00000341861.6:p.Ter464Cys
ENST00000378323.8:c.1518A>T	ENSP00000367574.4:p.Ter506Cys
ENST00000378324.6:c.1347A>T	ENSP00000367575.2:p.Ter449Cys
ENST00000403558.1:c.1632A>T	ENSP00000384420.1:p.Ter544Cys
ENST00000528996.1:c.704A>T	ENSP00000431226.1:n.704A>T
ENST00000531133.5:c.1004A>T	ENSP00000435431.1:n.1004A>T
ENST00000531797.5:c.*528A>T	ENSP00000432554.1:n.*528A>T
ENST00000619430.1:c.634A>T	ENSP00000478572.1:n.634A>T
NM_000062.2:c.1503A>T , LRG_105t1:c.1503A>T	NP_000053.2:p.Ter501Cys
NM_001032295.1:c.1503A>T	NP_001027466.1:p.Ter501Cys
NM_000062.3:c.1503A>T MANE Select	NP_000053.2:p.Ter501Cys
NM_001032295.2:c.1503A>T	NP_001027466.1:p.Ter501Cys