Canonical Allele Identifier: CA678628980
Gene: SERPING1 HGNC NCBI

Linked Data

dbSNP Id: rs1180026235

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57610771A>C , CM000673.2:g.57610771A>C GRCh38
NC_000011.9:g.57378244A>C , CM000673.1:g.57378244A>C GRCh37
NC_000011.8:g.57134820A>C NCBI36
NG_009625.1:g.18218A>C , LRG_105:g.18218A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000278407.9:c.1030-946A>C MANE Select ENSP00000278407.4:n.1030-946A>C
ENST00000528996.2:c.59-955A>C ENSP00000431226.2:n.59-955A>C
ENST00000531605.2:c.*806-946A>C ENSP00000503752.1:n.*806-946A>C
ENST00000619430.2:c.826-946A>C ENSP00000478572.2:n.826-946A>C
ENST00000676670.1:c.1030-946A>C ENSP00000504807.1:n.1030-946A>C
ENST00000676741.1:n.2112-946A>C
ENST00000677624.1:c.*450-946A>C ENSP00000503979.1:n.*450-946A>C
ENST00000677625.1:c.1030-1000A>C ENSP00000502857.1:n.1030-1000A>C
ENST00000677856.1:n.1283-946A>C
ENST00000677915.1:c.686-946A>C ENSP00000503118.1:n.686-946A>C
ENST00000678533.1:c.*584-946A>C ENSP00000503873.1:n.*584-946A>C
ENST00000678592.1:c.1119-946A>C ENSP00000504424.1:n.1119-946A>C
ENST00000278407.8:c.1030-946A>C ENSP00000278407.4:n.1030-946A>C
ENST00000340687.10:c.1030-1057A>C ENSP00000341861.6:n.1030-1057A>C
ENST00000378323.8:c.1045-946A>C ENSP00000367574.4:n.1045-946A>C
ENST00000378324.6:c.874-946A>C ENSP00000367575.2:n.874-946A>C
ENST00000403558.1:c.1159-946A>C ENSP00000384420.1:n.1159-946A>C
ENST00000528996.1:c.231-946A>C ENSP00000431226.1:n.231-946A>C
ENST00000531133.5:c.531-946A>C ENSP00000435431.1:n.531-946A>C
ENST00000531797.5:c.*55-946A>C ENSP00000432554.1:n.*55-946A>C
ENST00000619430.1:c.349-1134A>C ENSP00000478572.1:n.349-1134A>C
NM_000062.2:c.1030-946A>C , LRG_105t1:c.1030-946A>C NP_000053.2:n.1030-946A>C
NM_001032295.1:c.1030-946A>C NP_001027466.1:n.1030-946A>C
NM_000062.3:c.1030-946A>C MANE Select NP_000053.2:n.1030-946A>C
NM_001032295.2:c.1030-946A>C NP_001027466.1:n.1030-946A>C