Canonical Allele Identifier: CA938330450
Gene: SERPING1 HGNC NCBI

Linked Data

dbSNP Id: rs1945408209

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57606266C>T , CM000673.2:g.57606266C>T GRCh38
NC_000011.9:g.57373739C>T , CM000673.1:g.57373739C>T GRCh37
NC_000011.8:g.57130315C>T NCBI36
NG_009625.1:g.13713C>T , LRG_105:g.13713C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.889+53C>T MANE Select ENSP00000278407.4:n.889+53C>T
ENST00000528996.2:c.59-5460C>T ENSP00000431226.2:n.59-5460C>T
ENST00000531605.2:c.*665+53C>T ENSP00000503752.1:n.*665+53C>T
ENST00000619430.2:c.686-142C>T ENSP00000478572.2:n.686-142C>T
ENST00000676670.1:c.889+53C>T ENSP00000504807.1:n.889+53C>T
ENST00000676741.1:n.1971+53C>T
ENST00000677624.1:c.*309+53C>T ENSP00000503979.1:n.*309+53C>T
ENST00000677625.1:c.889+53C>T ENSP00000502857.1:n.889+53C>T
ENST00000677856.1:n.1001C>T
ENST00000677915.1:c.685+4097C>T ENSP00000503118.1:n.685+4097C>T
ENST00000678533.1:c.*443+53C>T ENSP00000503873.1:n.*443+53C>T
ENST00000678592.1:c.889+53C>T ENSP00000504424.1:n.889+53C>T
ENST00000278407.8:c.889+53C>T ENSP00000278407.4:n.889+53C>T
ENST00000340687.10:c.889+53C>T ENSP00000341861.6:n.889+53C>T
ENST00000378323.8:c.904+53C>T ENSP00000367574.4:n.904+53C>T
ENST00000378324.6:c.733+53C>T ENSP00000367575.2:n.733+53C>T
ENST00000403558.1:c.991+53C>T ENSP00000384420.1:n.991+53C>T
ENST00000531133.5:c.390+53C>T ENSP00000435431.1:n.390+53C>T
ENST00000531797.5:c.*54+4097C>T ENSP00000432554.1:n.*54+4097C>T
ENST00000619430.1:c.349-5639C>T ENSP00000478572.1:n.349-5639C>T
NM_000062.2:c.889+53C>T , LRG_105t1:c.889+53C>T NP_000053.2:n.889+53C>T
NM_001032295.1:c.889+53C>T NP_001027466.1:n.889+53C>T
NM_000062.3:c.889+53C>T MANE Select NP_000053.2:n.889+53C>T
NM_001032295.2:c.889+53C>T NP_001027466.1:n.889+53C>T