Canonical Allele Identifier: CA16619349
Gene: SERPING1 HGNC NCBI

Linked Data

ClinVar Variation Id: 418660
ClinVar RCV Id: RCV000485353
dbSNP Id: rs1064793350

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57600339C>T , CM000673.2:g.57600339C>T GRCh38
NC_000011.9:g.57367812C>T , CM000673.1:g.57367812C>T GRCh37
NC_000011.8:g.57124388C>T NCBI36
NG_009625.1:g.7786C>T , LRG_105:g.7786C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000278407.9:c.512C>T MANE Select ENSP00000278407.4:p.Pro171Leu
ENST00000528996.2:c.58+2011C>T ENSP00000431226.2:n.58+2011C>T
ENST00000531605.2:c.52-1696C>T ENSP00000503752.1:n.52-1696C>T
ENST00000619430.2:c.512C>T ENSP00000478572.2:p.Pro171Leu
ENST00000676670.1:c.512C>T ENSP00000504807.1:p.Pro171Leu
ENST00000676741.1:n.1594C>T
ENST00000677275.1:n.499C>T
ENST00000677624.1:c.512C>T ENSP00000503979.1:p.Pro171Leu
ENST00000677625.1:c.512C>T ENSP00000502857.1:p.Pro171Leu
ENST00000677856.1:n.571C>T
ENST00000677915.1:c.512C>T ENSP00000503118.1:p.Pro171Leu
ENST00000678533.1:c.52-1696C>T ENSP00000503873.1:n.52-1696C>T
ENST00000678592.1:c.512C>T ENSP00000504424.1:p.Pro171Leu
ENST00000278407.8:c.512C>T ENSP00000278407.4:p.Pro171Leu
ENST00000340687.10:c.512C>T ENSP00000341861.6:p.Pro171Leu
ENST00000378323.8:c.527C>T ENSP00000367574.4:p.Pro176Leu
ENST00000378324.6:c.356C>T ENSP00000367575.2:p.Pro119Leu
ENST00000403558.1:c.614C>T ENSP00000384420.1:p.Pro205Leu
ENST00000531133.5:c.52-1696C>T ENSP00000435431.1:n.52-1696C>T
ENST00000531797.5:c.52-1696C>T ENSP00000432554.1:n.52-1696C>T
ENST00000619430.1:c.348+164C>T ENSP00000478572.1:n.348+164C>T
NM_000062.2:c.512C>T , LRG_105t1:c.512C>T NP_000053.2:p.Pro171Leu
NM_001032295.1:c.512C>T NP_001027466.1:p.Pro171Leu
NM_000062.3:c.512C>T MANE Select NP_000053.2:p.Pro171Leu
NM_001032295.2:c.512C>T NP_001027466.1:p.Pro171Leu