Canonical Allele Identifier: CA1975539181
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57614440G= , CM000673.2:g.57614440G= GRCh38
NC_000011.9:g.57381913G= , CM000673.1:g.57381913G= GRCh37
NC_000011.8:g.57138489G= NCBI36
NG_009625.1:g.21887G= , LRG_105:g.21887G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.1362G= MANE Select ENSP00000278407.4:p.Val454=
ENST00000528996.2:c.*259G= ENSP00000431226.2:n.*259G=
ENST00000531605.2:c.*1138G= ENSP00000503752.1:n.*1138G=
ENST00000619430.2:c.1158G= ENSP00000478572.2:p.Val386=
ENST00000676670.1:c.1362G= ENSP00000504807.1:p.Val454=
ENST00000676741.1:n.2444G=
ENST00000677624.1:c.*782G= ENSP00000503979.1:n.*782G=
ENST00000677625.1:c.1308G= ENSP00000502857.1:p.Val436=
ENST00000677856.1:n.1615G=
ENST00000677915.1:c.*259G= ENSP00000503118.1:n.*259G=
ENST00000678533.1:c.*916G= ENSP00000503873.1:n.*916G=
ENST00000678592.1:c.*302G= ENSP00000504424.1:n.*302G=
ENST00000278407.8:c.1362G= ENSP00000278407.4:p.Val454=
ENST00000340687.10:c.1251G= ENSP00000341861.6:p.Val417=
ENST00000378323.8:c.1377G= ENSP00000367574.4:p.Val459=
ENST00000378324.6:c.1206G= ENSP00000367575.2:p.Val402=
ENST00000403558.1:c.1491G= ENSP00000384420.1:p.Val497=
ENST00000528996.1:c.563G= ENSP00000431226.1:n.563G=
ENST00000530113.1:n.819G=
ENST00000531133.5:c.863G= ENSP00000435431.1:n.863G=
ENST00000531797.5:c.*387G= ENSP00000432554.1:n.*387G=
ENST00000619430.1:c.493G= ENSP00000478572.1:n.493G=
NM_000062.2:c.1362G= , LRG_105t1:c.1362G= NP_000053.2:p.Val454=
NM_001032295.1:c.1362G= NP_001027466.1:p.Val454=
NM_000062.3:c.1362G= MANE Select NP_000053.2:p.Val454=
NM_001032295.2:c.1362G= NP_001027466.1:p.Val454=