Canonical Allele Identifier: CA2613603994
Gene: SERPING1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57614739G>A , CM000673.2:g.57614739G>A GRCh38
NC_000011.9:g.57382212G>A , CM000673.1:g.57382212G>A GRCh37
NC_000011.8:g.57138788G>A NCBI36
NG_009625.1:g.22186G>A , LRG_105:g.22186G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.*158G>A MANE Select ENSP00000278407.4:n.*158G>A
ENST00000528996.2:c.*558G>A ENSP00000431226.2:n.*558G>A
ENST00000531605.2:c.*1437G>A ENSP00000503752.1:n.*1437G>A
ENST00000619430.2:c.*158G>A ENSP00000478572.2:n.*158G>A
ENST00000676670.1:c.*15+143G>A ENSP00000504807.1:n.*15+143G>A
ENST00000676741.1:n.2743G>A
ENST00000677624.1:c.*1081G>A ENSP00000503979.1:n.*1081G>A
ENST00000677625.1:c.*158G>A ENSP00000502857.1:n.*158G>A
ENST00000677856.1:n.1914G>A
ENST00000677915.1:c.*558G>A ENSP00000503118.1:n.*558G>A
ENST00000678533.1:c.*1072+143G>A ENSP00000503873.1:n.*1072+143G>A
ENST00000678592.1:c.*601G>A ENSP00000504424.1:n.*601G>A
ENST00000278407.8:c.*158G>A ENSP00000278407.4:n.*158G>A
ENST00000340687.10:c.*158G>A ENSP00000341861.6:n.*158G>A
ENST00000378323.8:c.*158G>A ENSP00000367574.4:n.*158G>A
ENST00000378324.6:c.*158G>A ENSP00000367575.2:n.*158G>A
ENST00000403558.1:c.*158G>A ENSP00000384420.1:n.*158G>A
ENST00000528996.1:c.862G>A ENSP00000431226.1:n.862G>A
ENST00000531797.5:c.*686G>A ENSP00000432554.1:n.*686G>A
NM_000062.2:c.*158G>A , LRG_105t1:c.*158G>A NP_000053.2:n.*158G>A
NM_001032295.1:c.*158G>A NP_001027466.1:n.*158G>A
NM_000062.3:c.*158G>A MANE Select NP_000053.2:n.*158G>A
NM_001032295.2:c.*158G>A NP_001027466.1:n.*158G>A