Canonical Allele Identifier: CA10631046
Community Standard Title: NM_000062.3(SERPING1):c.135C>T (p.Val45=)
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57599962C>T , CM000673.2:g.57599962C>T GRCh38
NC_000011.9:g.57367435C>T , CM000673.1:g.57367435C>T GRCh37
NC_000011.8:g.57124011C>T NCBI36
NG_009625.1:g.7409C>T , LRG_105:g.7409C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000062.3:c.135C>T MANE Select NP_000053.2:p.Val45=
ENST00000278407.9:c.135C>T MANE Select ENSP00000278407.4:p.Val45=
NM_000062.2:c.135C>T , LRG_105t1:c.135C>T NP_000053.2:p.Val45=
NM_001032295.1:c.135C>T NP_001027466.1:p.Val45=
NM_001032295.2:c.135C>T NP_001027466.1:p.Val45=
ENST00000278407.8:c.135C>T ENSP00000278407.4:p.Val45=
ENST00000340687.10:c.135C>T ENSP00000341861.6:p.Val45=
ENST00000378323.8:c.150C>T ENSP00000367574.4:p.Val50=
ENST00000378324.6:c.-22C>T ENSP00000367575.2:n.-22C>T
ENST00000403558.1:c.237C>T ENSP00000384420.1:p.Val79=
ENST00000405496.5:c.135C>T ENSP00000384561.1:p.Val45=
ENST00000457869.1:c.237C>T ENSP00000399746.1:p.Val79=
ENST00000528996.2:c.58+1634C>T ENSP00000431226.2:n.58+1634C>T
ENST00000531133.5:c.51+1641C>T ENSP00000435431.1:n.51+1641C>T
ENST00000531605.2:c.51+1641C>T ENSP00000503752.1:n.51+1641C>T
ENST00000531797.5:c.51+1641C>T ENSP00000432554.1:n.51+1641C>T
ENST00000619430.1:c.135C>T ENSP00000478572.1:p.Val45=
ENST00000619430.2:c.135C>T ENSP00000478572.2:p.Val45=
ENST00000676670.1:c.135C>T ENSP00000504807.1:p.Val45=
ENST00000676741.1:n.1217C>T
ENST00000677275.1:n.122C>T
ENST00000677624.1:c.135C>T ENSP00000503979.1:p.Val45=
ENST00000677625.1:c.135C>T ENSP00000502857.1:p.Val45=
ENST00000677856.1:n.194C>T
ENST00000677915.1:c.135C>T ENSP00000503118.1:p.Val45=
ENST00000678533.1:c.51+1641C>T ENSP00000503873.1:n.51+1641C>T
ENST00000678592.1:c.135C>T ENSP00000504424.1:p.Val45=