Canonical Allele Identifier: CA6007987
Gene: SERPING1 HGNC NCBI

Linked Data

ClinVar Variation Id: 305020
dbSNP Id: rs11546660

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57599994T>C , CM000673.2:g.57599994T>C GRCh38
NC_000011.9:g.57367467T>C , CM000673.1:g.57367467T>C GRCh37
NC_000011.8:g.57124043T>C NCBI36
NG_009625.1:g.7441T>C , LRG_105:g.7441T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000278407.9:c.167T>C MANE Select ENSP00000278407.4:p.Val56Ala
ENST00000528996.2:c.58+1666T>C ENSP00000431226.2:n.58+1666T>C
ENST00000531605.2:c.51+1673T>C ENSP00000503752.1:n.51+1673T>C
ENST00000619430.2:c.167T>C ENSP00000478572.2:p.Val56Ala
ENST00000676670.1:c.167T>C ENSP00000504807.1:p.Val56Ala
ENST00000676741.1:n.1249T>C
ENST00000677275.1:n.154T>C
ENST00000677624.1:c.167T>C ENSP00000503979.1:p.Val56Ala
ENST00000677625.1:c.167T>C ENSP00000502857.1:p.Val56Ala
ENST00000677856.1:n.226T>C
ENST00000677915.1:c.167T>C ENSP00000503118.1:p.Val56Ala
ENST00000678533.1:c.51+1673T>C ENSP00000503873.1:n.51+1673T>C
ENST00000678592.1:c.167T>C ENSP00000504424.1:p.Val56Ala
ENST00000278407.8:c.167T>C ENSP00000278407.4:p.Val56Ala
ENST00000340687.10:c.167T>C ENSP00000341861.6:p.Val56Ala
ENST00000378323.8:c.182T>C ENSP00000367574.4:p.Val61Ala
ENST00000378324.6:c.11T>C ENSP00000367575.2:p.Val4Ala
ENST00000403558.1:c.269T>C ENSP00000384420.1:p.Val90Ala
ENST00000405496.5:c.167T>C ENSP00000384561.1:p.Val56Ala
ENST00000457869.1:c.269T>C ENSP00000399746.1:p.Val90Ala
ENST00000531133.5:c.51+1673T>C ENSP00000435431.1:n.51+1673T>C
ENST00000531797.5:c.51+1673T>C ENSP00000432554.1:n.51+1673T>C
ENST00000619430.1:c.167T>C ENSP00000478572.1:p.Val56Ala
NM_000062.2:c.167T>C , LRG_105t1:c.167T>C NP_000053.2:p.Val56Ala
NM_001032295.1:c.167T>C NP_001027466.1:p.Val56Ala
NM_000062.3:c.167T>C MANE Select NP_000053.2:p.Val56Ala
NM_001032295.2:c.167T>C NP_001027466.1:p.Val56Ala