Canonical Allele Identifier: CA223056843
Gene: SERPING1 HGNC NCBI

Linked Data

dbSNP Id: rs1054161888

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57610829T>C , CM000673.2:g.57610829T>C GRCh38
NC_000011.9:g.57378302T>C , CM000673.1:g.57378302T>C GRCh37
NC_000011.8:g.57134878T>C NCBI36
NG_009625.1:g.18276T>C , LRG_105:g.18276T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.1030-888T>C MANE Select ENSP00000278407.4:n.1030-888T>C
ENST00000528996.2:c.59-897T>C ENSP00000431226.2:n.59-897T>C
ENST00000531605.2:c.*806-888T>C ENSP00000503752.1:n.*806-888T>C
ENST00000619430.2:c.826-888T>C ENSP00000478572.2:n.826-888T>C
ENST00000676670.1:c.1030-888T>C ENSP00000504807.1:n.1030-888T>C
ENST00000676741.1:n.2112-888T>C
ENST00000677624.1:c.*450-888T>C ENSP00000503979.1:n.*450-888T>C
ENST00000677625.1:c.1030-942T>C ENSP00000502857.1:n.1030-942T>C
ENST00000677856.1:n.1283-888T>C
ENST00000677915.1:c.686-888T>C ENSP00000503118.1:n.686-888T>C
ENST00000678533.1:c.*584-888T>C ENSP00000503873.1:n.*584-888T>C
ENST00000678592.1:c.1119-888T>C ENSP00000504424.1:n.1119-888T>C
ENST00000278407.8:c.1030-888T>C ENSP00000278407.4:n.1030-888T>C
ENST00000340687.10:c.1030-999T>C ENSP00000341861.6:n.1030-999T>C
ENST00000378323.8:c.1045-888T>C ENSP00000367574.4:n.1045-888T>C
ENST00000378324.6:c.874-888T>C ENSP00000367575.2:n.874-888T>C
ENST00000403558.1:c.1159-888T>C ENSP00000384420.1:n.1159-888T>C
ENST00000528996.1:c.231-888T>C ENSP00000431226.1:n.231-888T>C
ENST00000531133.5:c.531-888T>C ENSP00000435431.1:n.531-888T>C
ENST00000531797.5:c.*55-888T>C ENSP00000432554.1:n.*55-888T>C
ENST00000619430.1:c.349-1076T>C ENSP00000478572.1:n.349-1076T>C
NM_000062.2:c.1030-888T>C , LRG_105t1:c.1030-888T>C NP_000053.2:n.1030-888T>C
NM_001032295.1:c.1030-888T>C NP_001027466.1:n.1030-888T>C
NM_000062.3:c.1030-888T>C MANE Select NP_000053.2:n.1030-888T>C
NM_001032295.2:c.1030-888T>C NP_001027466.1:n.1030-888T>C