Canonical Allele Identifier: CA380690339

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381845G>T (hg19) ; chr11:g.57614372G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614372G>T , CM000673.2:g.57614372G>T	GRCh38
NC_000011.9:g.57381845G>T , CM000673.1:g.57381845G>T	GRCh37
NC_000011.8:g.57138421G>T	NCBI36
NG_009625.1:g.21819G>T , LRG_105:g.21819G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.1294G>T MANE Select	ENSP00000278407.4:p.Glu432Ter
ENST00000528996.2:c.*191G>T	ENSP00000431226.2:n.*191G>T
ENST00000531605.2:c.*1070G>T	ENSP00000503752.1:n.*1070G>T
ENST00000619430.2:c.1090G>T	ENSP00000478572.2:p.Glu364Ter
ENST00000676670.1:c.1294G>T	ENSP00000504807.1:p.Glu432Ter
ENST00000676741.1:n.2376G>T
ENST00000677624.1:c.*714G>T	ENSP00000503979.1:n.*714G>T
ENST00000677625.1:c.1240G>T	ENSP00000502857.1:p.Glu414Ter
ENST00000677856.1:n.1547G>T
ENST00000677915.1:c.*191G>T	ENSP00000503118.1:n.*191G>T
ENST00000678533.1:c.*848G>T	ENSP00000503873.1:n.*848G>T
ENST00000678592.1:c.*234G>T	ENSP00000504424.1:n.*234G>T
ENST00000278407.8:c.1294G>T	ENSP00000278407.4:p.Glu432Ter
ENST00000340687.10:c.1183G>T	ENSP00000341861.6:p.Glu395Ter
ENST00000378323.8:c.1309G>T	ENSP00000367574.4:p.Glu437Ter
ENST00000378324.6:c.1138G>T	ENSP00000367575.2:p.Glu380Ter
ENST00000403558.1:c.1423G>T	ENSP00000384420.1:p.Glu475Ter
ENST00000528996.1:c.495G>T	ENSP00000431226.1:n.495G>T
ENST00000530113.1:n.751G>T
ENST00000531133.5:c.795G>T	ENSP00000435431.1:n.795G>T
ENST00000531797.5:c.*319G>T	ENSP00000432554.1:n.*319G>T
ENST00000619430.1:c.425G>T	ENSP00000478572.1:n.425G>T
NM_000062.2:c.1294G>T , LRG_105t1:c.1294G>T	NP_000053.2:p.Glu432Ter
NM_001032295.1:c.1294G>T	NP_001027466.1:p.Glu432Ter
NM_000062.3:c.1294G>T MANE Select	NP_000053.2:p.Glu432Ter
NM_001032295.2:c.1294G>T	NP_001027466.1:p.Glu432Ter