Canonical Allele Identifier: CA380690653

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381908G>T (hg19) ; chr11:g.57614435G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614435G>T , CM000673.2:g.57614435G>T	GRCh38
NC_000011.9:g.57381908G>T , CM000673.1:g.57381908G>T	GRCh37
NC_000011.8:g.57138484G>T	NCBI36
NG_009625.1:g.21882G>T , LRG_105:g.21882G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1357G>T MANE Select	ENSP00000278407.4:p.Gly453Trp
ENST00000528996.2:c.*254G>T	ENSP00000431226.2:n.*254G>T
ENST00000531605.2:c.*1133G>T	ENSP00000503752.1:n.*1133G>T
ENST00000619430.2:c.1153G>T	ENSP00000478572.2:p.Gly385Trp
ENST00000676670.1:c.1357G>T	ENSP00000504807.1:p.Gly453Trp
ENST00000676741.1:n.2439G>T
ENST00000677624.1:c.*777G>T	ENSP00000503979.1:n.*777G>T
ENST00000677625.1:c.1303G>T	ENSP00000502857.1:p.Gly435Trp
ENST00000677856.1:n.1610G>T
ENST00000677915.1:c.*254G>T	ENSP00000503118.1:n.*254G>T
ENST00000678533.1:c.*911G>T	ENSP00000503873.1:n.*911G>T
ENST00000678592.1:c.*297G>T	ENSP00000504424.1:n.*297G>T
ENST00000278407.8:c.1357G>T	ENSP00000278407.4:p.Gly453Trp
ENST00000340687.10:c.1246G>T	ENSP00000341861.6:p.Gly416Trp
ENST00000378323.8:c.1372G>T	ENSP00000367574.4:p.Gly458Trp
ENST00000378324.6:c.1201G>T	ENSP00000367575.2:p.Gly401Trp
ENST00000403558.1:c.1486G>T	ENSP00000384420.1:p.Gly496Trp
ENST00000528996.1:c.558G>T	ENSP00000431226.1:n.558G>T
ENST00000530113.1:n.814G>T
ENST00000531133.5:c.858G>T	ENSP00000435431.1:n.858G>T
ENST00000531797.5:c.*382G>T	ENSP00000432554.1:n.*382G>T
ENST00000619430.1:c.488G>T	ENSP00000478572.1:n.488G>T
NM_000062.2:c.1357G>T , LRG_105t1:c.1357G>T	NP_000053.2:p.Gly453Trp
NM_001032295.1:c.1357G>T	NP_001027466.1:p.Gly453Trp
NM_000062.3:c.1357G>T MANE Select	NP_000053.2:p.Gly453Trp
NM_001032295.2:c.1357G>T	NP_001027466.1:p.Gly453Trp