Canonical Allele Identifier: CA938332774
Gene: SERPING1 HGNC NCBI

Linked Data

dbSNP Id: rs1945468463

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57610764T>C , CM000673.2:g.57610764T>C GRCh38
NC_000011.9:g.57378237T>C , CM000673.1:g.57378237T>C GRCh37
NC_000011.8:g.57134813T>C NCBI36
NG_009625.1:g.18211T>C , LRG_105:g.18211T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000278407.9:c.1030-953T>C MANE Select ENSP00000278407.4:n.1030-953T>C
ENST00000528996.2:c.59-962T>C ENSP00000431226.2:n.59-962T>C
ENST00000531605.2:c.*806-953T>C ENSP00000503752.1:n.*806-953T>C
ENST00000619430.2:c.826-953T>C ENSP00000478572.2:n.826-953T>C
ENST00000676670.1:c.1030-953T>C ENSP00000504807.1:n.1030-953T>C
ENST00000676741.1:n.2112-953T>C
ENST00000677624.1:c.*450-953T>C ENSP00000503979.1:n.*450-953T>C
ENST00000677625.1:c.1030-1007T>C ENSP00000502857.1:n.1030-1007T>C
ENST00000677856.1:n.1283-953T>C
ENST00000677915.1:c.686-953T>C ENSP00000503118.1:n.686-953T>C
ENST00000678533.1:c.*584-953T>C ENSP00000503873.1:n.*584-953T>C
ENST00000678592.1:c.1119-953T>C ENSP00000504424.1:n.1119-953T>C
ENST00000278407.8:c.1030-953T>C ENSP00000278407.4:n.1030-953T>C
ENST00000340687.10:c.1030-1064T>C ENSP00000341861.6:n.1030-1064T>C
ENST00000378323.8:c.1045-953T>C ENSP00000367574.4:n.1045-953T>C
ENST00000378324.6:c.874-953T>C ENSP00000367575.2:n.874-953T>C
ENST00000403558.1:c.1159-953T>C ENSP00000384420.1:n.1159-953T>C
ENST00000528996.1:c.231-953T>C ENSP00000431226.1:n.231-953T>C
ENST00000531133.5:c.531-953T>C ENSP00000435431.1:n.531-953T>C
ENST00000531797.5:c.*55-953T>C ENSP00000432554.1:n.*55-953T>C
ENST00000619430.1:c.349-1141T>C ENSP00000478572.1:n.349-1141T>C
NM_000062.2:c.1030-953T>C , LRG_105t1:c.1030-953T>C NP_000053.2:n.1030-953T>C
NM_001032295.1:c.1030-953T>C NP_001027466.1:n.1030-953T>C
NM_000062.3:c.1030-953T>C MANE Select NP_000053.2:n.1030-953T>C
NM_001032295.2:c.1030-953T>C NP_001027466.1:n.1030-953T>C