Canonical Allele Identifier: CA2613603303
Gene: SERPING1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57614589A>G , CM000673.2:g.57614589A>G GRCh38
NC_000011.9:g.57382062A>G , CM000673.1:g.57382062A>G GRCh37
NC_000011.8:g.57138638A>G NCBI36
NG_009625.1:g.22036A>G , LRG_105:g.22036A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.*8A>G MANE Select ENSP00000278407.4:n.*8A>G
ENST00000528996.2:c.*408A>G ENSP00000431226.2:n.*408A>G
ENST00000531605.2:c.*1287A>G ENSP00000503752.1:n.*1287A>G
ENST00000619430.2:c.*8A>G ENSP00000478572.2:n.*8A>G
ENST00000676670.1:c.*8A>G ENSP00000504807.1:n.*8A>G
ENST00000676741.1:n.2593A>G
ENST00000677624.1:c.*931A>G ENSP00000503979.1:n.*931A>G
ENST00000677625.1:c.*8A>G ENSP00000502857.1:n.*8A>G
ENST00000677856.1:n.1764A>G
ENST00000677915.1:c.*408A>G ENSP00000503118.1:n.*408A>G
ENST00000678533.1:c.*1065A>G ENSP00000503873.1:n.*1065A>G
ENST00000678592.1:c.*451A>G ENSP00000504424.1:n.*451A>G
ENST00000278407.8:c.*8A>G ENSP00000278407.4:n.*8A>G
ENST00000340687.10:c.*8A>G ENSP00000341861.6:n.*8A>G
ENST00000378323.8:c.*8A>G ENSP00000367574.4:n.*8A>G
ENST00000378324.6:c.*8A>G ENSP00000367575.2:n.*8A>G
ENST00000403558.1:c.*8A>G ENSP00000384420.1:n.*8A>G
ENST00000528996.1:c.712A>G ENSP00000431226.1:n.712A>G
ENST00000531797.5:c.*536A>G ENSP00000432554.1:n.*536A>G
NM_000062.2:c.*8A>G , LRG_105t1:c.*8A>G NP_000053.2:n.*8A>G
NM_001032295.1:c.*8A>G NP_001027466.1:n.*8A>G
NM_000062.3:c.*8A>G MANE Select NP_000053.2:n.*8A>G
NM_001032295.2:c.*8A>G NP_001027466.1:n.*8A>G