Canonical Allele Identifier: CA380690313

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381836G>T (hg19) ; chr11:g.57614363G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614363G>T , CM000673.2:g.57614363G>T	GRCh38
NC_000011.9:g.57381836G>T , CM000673.1:g.57381836G>T	GRCh37
NC_000011.8:g.57138412G>T	NCBI36
NG_009625.1:g.21810G>T , LRG_105:g.21810G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.1285G>T MANE Select	ENSP00000278407.4:p.Gly429Trp
ENST00000528996.2:c.*182G>T	ENSP00000431226.2:n.*182G>T
ENST00000531605.2:c.*1061G>T	ENSP00000503752.1:n.*1061G>T
ENST00000619430.2:c.1081G>T	ENSP00000478572.2:p.Gly361Trp
ENST00000676670.1:c.1285G>T	ENSP00000504807.1:p.Gly429Trp
ENST00000676741.1:n.2367G>T
ENST00000677624.1:c.*705G>T	ENSP00000503979.1:n.*705G>T
ENST00000677625.1:c.1231G>T	ENSP00000502857.1:p.Gly411Trp
ENST00000677856.1:n.1538G>T
ENST00000677915.1:c.*182G>T	ENSP00000503118.1:n.*182G>T
ENST00000678533.1:c.*839G>T	ENSP00000503873.1:n.*839G>T
ENST00000678592.1:c.*225G>T	ENSP00000504424.1:n.*225G>T
ENST00000278407.8:c.1285G>T	ENSP00000278407.4:p.Gly429Trp
ENST00000340687.10:c.1174G>T	ENSP00000341861.6:p.Gly392Trp
ENST00000378323.8:c.1300G>T	ENSP00000367574.4:p.Gly434Trp
ENST00000378324.6:c.1129G>T	ENSP00000367575.2:p.Gly377Trp
ENST00000403558.1:c.1414G>T	ENSP00000384420.1:p.Gly472Trp
ENST00000528996.1:c.486G>T	ENSP00000431226.1:n.486G>T
ENST00000530113.1:n.742G>T
ENST00000531133.5:c.786G>T	ENSP00000435431.1:n.786G>T
ENST00000531797.5:c.*310G>T	ENSP00000432554.1:n.*310G>T
ENST00000619430.1:c.416G>T	ENSP00000478572.1:n.416G>T
NM_000062.2:c.1285G>T , LRG_105t1:c.1285G>T	NP_000053.2:p.Gly429Trp
NM_001032295.1:c.1285G>T	NP_001027466.1:p.Gly429Trp
NM_000062.3:c.1285G>T MANE Select	NP_000053.2:p.Gly429Trp
NM_001032295.2:c.1285G>T	NP_001027466.1:p.Gly429Trp