Canonical Allele Identifier: CA2613602629
Gene: SERPING1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57614248G>T , CM000673.2:g.57614248G>T GRCh38
NC_000011.9:g.57381721G>T , CM000673.1:g.57381721G>T GRCh37
NC_000011.8:g.57138297G>T NCBI36
NG_009625.1:g.21695G>T , LRG_105:g.21695G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.1250-80G>T MANE Select ENSP00000278407.4:n.1250-80G>T
ENST00000528996.2:c.*147-80G>T ENSP00000431226.2:n.*147-80G>T
ENST00000531605.2:c.*1026-80G>T ENSP00000503752.1:n.*1026-80G>T
ENST00000619430.2:c.1046-80G>T ENSP00000478572.2:n.1046-80G>T
ENST00000676670.1:c.1250-80G>T ENSP00000504807.1:n.1250-80G>T
ENST00000676741.1:n.2332-80G>T
ENST00000677624.1:c.*670-80G>T ENSP00000503979.1:n.*670-80G>T
ENST00000677625.1:c.1196-80G>T ENSP00000502857.1:n.1196-80G>T
ENST00000677856.1:n.1503-80G>T
ENST00000677915.1:c.*147-80G>T ENSP00000503118.1:n.*147-80G>T
ENST00000678533.1:c.*804-80G>T ENSP00000503873.1:n.*804-80G>T
ENST00000678592.1:c.*190-80G>T ENSP00000504424.1:n.*190-80G>T
ENST00000278407.8:c.1250-80G>T ENSP00000278407.4:n.1250-80G>T
ENST00000340687.10:c.1139-80G>T ENSP00000341861.6:n.1139-80G>T
ENST00000378323.8:c.1265-80G>T ENSP00000367574.4:n.1265-80G>T
ENST00000378324.6:c.1094-80G>T ENSP00000367575.2:n.1094-80G>T
ENST00000403558.1:c.1379-80G>T ENSP00000384420.1:n.1379-80G>T
ENST00000528996.1:c.451-80G>T ENSP00000431226.1:n.451-80G>T
ENST00000530113.1:n.707-80G>T
ENST00000531133.5:c.751-80G>T ENSP00000435431.1:n.751-80G>T
ENST00000531797.5:c.*275-80G>T ENSP00000432554.1:n.*275-80G>T
ENST00000619430.1:c.381-80G>T ENSP00000478572.1:n.381-80G>T
NM_000062.2:c.1250-80G>T , LRG_105t1:c.1250-80G>T NP_000053.2:n.1250-80G>T
NM_001032295.1:c.1250-80G>T NP_001027466.1:n.1250-80G>T
NM_000062.3:c.1250-80G>T MANE Select NP_000053.2:n.1250-80G>T
NM_001032295.2:c.1250-80G>T NP_001027466.1:n.1250-80G>T