Canonical Allele Identifier: CA474806934
Gene: SERPING1 HGNC NCBI

Linked Data

COSMIC: COSM928665
MyVariant Identifiers: chr11:g.57381994C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57614521C>T , CM000673.2:g.57614521C>T GRCh38
NC_000011.9:g.57381994C>T , CM000673.1:g.57381994C>T GRCh37
NC_000011.8:g.57138570C>T NCBI36
NG_009625.1:g.21968C>T , LRG_105:g.21968C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.1443C>T MANE Select ENSP00000278407.4:p.Leu481=
ENST00000528996.2:c.*340C>T ENSP00000431226.2:n.*340C>T
ENST00000531605.2:c.*1219C>T ENSP00000503752.1:n.*1219C>T
ENST00000619430.2:c.1239C>T ENSP00000478572.2:p.Leu413=
ENST00000676670.1:c.1443C>T ENSP00000504807.1:p.Leu481=
ENST00000676741.1:n.2525C>T
ENST00000677624.1:c.*863C>T ENSP00000503979.1:n.*863C>T
ENST00000677625.1:c.1389C>T ENSP00000502857.1:p.Leu463=
ENST00000677856.1:n.1696C>T
ENST00000677915.1:c.*340C>T ENSP00000503118.1:n.*340C>T
ENST00000678533.1:c.*997C>T ENSP00000503873.1:n.*997C>T
ENST00000678592.1:c.*383C>T ENSP00000504424.1:n.*383C>T
ENST00000278407.8:c.1443C>T ENSP00000278407.4:p.Leu481=
ENST00000340687.10:c.1332C>T ENSP00000341861.6:p.Leu444=
ENST00000378323.8:c.1458C>T ENSP00000367574.4:p.Leu486=
ENST00000378324.6:c.1287C>T ENSP00000367575.2:p.Leu429=
ENST00000403558.1:c.1572C>T ENSP00000384420.1:p.Leu524=
ENST00000528996.1:c.644C>T ENSP00000431226.1:n.644C>T
ENST00000530113.1:n.900C>T
ENST00000531133.5:c.944C>T ENSP00000435431.1:n.944C>T
ENST00000531797.5:c.*468C>T ENSP00000432554.1:n.*468C>T
ENST00000619430.1:c.574C>T ENSP00000478572.1:n.574C>T
NM_000062.2:c.1443C>T , LRG_105t1:c.1443C>T NP_000053.2:p.Leu481=
NM_001032295.1:c.1443C>T NP_001027466.1:p.Leu481=
NM_000062.3:c.1443C>T MANE Select NP_000053.2:p.Leu481=
NM_001032295.2:c.1443C>T NP_001027466.1:p.Leu481=