Canonical Allele Identifier: CA380690767

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381963T>A (hg19) ; chr11:g.57614490T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614490T>A , CM000673.2:g.57614490T>A	GRCh38
NC_000011.9:g.57381963T>A , CM000673.1:g.57381963T>A	GRCh37
NC_000011.8:g.57138539T>A	NCBI36
NG_009625.1:g.21937T>A , LRG_105:g.21937T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1412T>A MANE Select	ENSP00000278407.4:p.Phe471Tyr
ENST00000528996.2:c.*309T>A	ENSP00000431226.2:n.*309T>A
ENST00000531605.2:c.*1188T>A	ENSP00000503752.1:n.*1188T>A
ENST00000619430.2:c.1208T>A	ENSP00000478572.2:p.Phe403Tyr
ENST00000676670.1:c.1412T>A	ENSP00000504807.1:p.Phe471Tyr
ENST00000676741.1:n.2494T>A
ENST00000677624.1:c.*832T>A	ENSP00000503979.1:n.*832T>A
ENST00000677625.1:c.1358T>A	ENSP00000502857.1:p.Phe453Tyr
ENST00000677856.1:n.1665T>A
ENST00000677915.1:c.*309T>A	ENSP00000503118.1:n.*309T>A
ENST00000678533.1:c.*966T>A	ENSP00000503873.1:n.*966T>A
ENST00000678592.1:c.*352T>A	ENSP00000504424.1:n.*352T>A
ENST00000278407.8:c.1412T>A	ENSP00000278407.4:p.Phe471Tyr
ENST00000340687.10:c.1301T>A	ENSP00000341861.6:p.Phe434Tyr
ENST00000378323.8:c.1427T>A	ENSP00000367574.4:p.Phe476Tyr
ENST00000378324.6:c.1256T>A	ENSP00000367575.2:p.Phe419Tyr
ENST00000403558.1:c.1541T>A	ENSP00000384420.1:p.Phe514Tyr
ENST00000528996.1:c.613T>A	ENSP00000431226.1:n.613T>A
ENST00000530113.1:n.869T>A
ENST00000531133.5:c.913T>A	ENSP00000435431.1:n.913T>A
ENST00000531797.5:c.*437T>A	ENSP00000432554.1:n.*437T>A
ENST00000619430.1:c.543T>A	ENSP00000478572.1:n.543T>A
NM_000062.2:c.1412T>A , LRG_105t1:c.1412T>A	NP_000053.2:p.Phe471Tyr
NM_001032295.1:c.1412T>A	NP_001027466.1:p.Phe471Tyr
NM_000062.3:c.1412T>A MANE Select	NP_000053.2:p.Phe471Tyr
NM_001032295.2:c.1412T>A	NP_001027466.1:p.Phe471Tyr