Canonical Allele Identifier: CA380690973

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57382052T>G (hg19) ; chr11:g.57614579T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614579T>G , CM000673.2:g.57614579T>G	GRCh38
NC_000011.9:g.57382052T>G , CM000673.1:g.57382052T>G	GRCh37
NC_000011.8:g.57138628T>G	NCBI36
NG_009625.1:g.22026T>G , LRG_105:g.22026T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1501T>G MANE Select	ENSP00000278407.4:p.Ter501Gly
ENST00000528996.2:c.*398T>G	ENSP00000431226.2:n.*398T>G
ENST00000531605.2:c.*1277T>G	ENSP00000503752.1:n.*1277T>G
ENST00000619430.2:c.1297T>G	ENSP00000478572.2:p.Ter433Gly
ENST00000676670.1:c.1501T>G	ENSP00000504807.1:p.Ter501Gly
ENST00000676741.1:n.2583T>G
ENST00000677624.1:c.*921T>G	ENSP00000503979.1:n.*921T>G
ENST00000677625.1:c.1447T>G	ENSP00000502857.1:p.Ter483Gly
ENST00000677856.1:n.1754T>G
ENST00000677915.1:c.*398T>G	ENSP00000503118.1:n.*398T>G
ENST00000678533.1:c.*1055T>G	ENSP00000503873.1:n.*1055T>G
ENST00000678592.1:c.*441T>G	ENSP00000504424.1:n.*441T>G
ENST00000278407.8:c.1501T>G	ENSP00000278407.4:p.Ter501Gly
ENST00000340687.10:c.1390T>G	ENSP00000341861.6:p.Ter464Gly
ENST00000378323.8:c.1516T>G	ENSP00000367574.4:p.Ter506Gly
ENST00000378324.6:c.1345T>G	ENSP00000367575.2:p.Ter449Gly
ENST00000403558.1:c.1630T>G	ENSP00000384420.1:p.Ter544Gly
ENST00000528996.1:c.702T>G	ENSP00000431226.1:n.702T>G
ENST00000531133.5:c.1002T>G	ENSP00000435431.1:n.1002T>G
ENST00000531797.5:c.*526T>G	ENSP00000432554.1:n.*526T>G
ENST00000619430.1:c.632T>G	ENSP00000478572.1:n.632T>G
NM_000062.2:c.1501T>G , LRG_105t1:c.1501T>G	NP_000053.2:p.Ter501Gly
NM_001032295.1:c.1501T>G	NP_001027466.1:p.Ter501Gly
NM_000062.3:c.1501T>G MANE Select	NP_000053.2:p.Ter501Gly
NM_001032295.2:c.1501T>G	NP_001027466.1:p.Ter501Gly