Canonical Allele Identifier: CA1975537098
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57611834A= , CM000673.2:g.57611834A= GRCh38
NC_000011.9:g.57379307A= , CM000673.1:g.57379307A= GRCh37
NC_000011.8:g.57135883A= NCBI36
NG_009625.1:g.19281A= , LRG_105:g.19281A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.1147A= MANE Select ENSP00000278407.4:p.Met383=
ENST00000528996.2:c.*44A= ENSP00000431226.2:n.*44A=
ENST00000531605.2:c.*923A= ENSP00000503752.1:n.*923A=
ENST00000619430.2:c.943A= ENSP00000478572.2:p.Met315=
ENST00000676670.1:c.1147A= ENSP00000504807.1:p.Met383=
ENST00000676741.1:n.2229A=
ENST00000677624.1:c.*567A= ENSP00000503979.1:n.*567A=
ENST00000677625.1:c.1093A= ENSP00000502857.1:p.Met365=
ENST00000677856.1:n.1400A=
ENST00000677915.1:c.*44A= ENSP00000503118.1:n.*44A=
ENST00000678533.1:c.*701A= ENSP00000503873.1:n.*701A=
ENST00000678592.1:c.*87A= ENSP00000504424.1:n.*87A=
ENST00000278407.8:c.1147A= ENSP00000278407.4:p.Met383=
ENST00000340687.10:c.1036A= ENSP00000341861.6:p.Met346=
ENST00000378323.8:c.1162A= ENSP00000367574.4:p.Met388=
ENST00000378324.6:c.991A= ENSP00000367575.2:p.Met331=
ENST00000403558.1:c.1276A= ENSP00000384420.1:p.Met426=
ENST00000528996.1:c.348A= ENSP00000431226.1:n.348A=
ENST00000530113.1:n.604A=
ENST00000531133.5:c.648A= ENSP00000435431.1:n.648A=
ENST00000531797.5:c.*172A= ENSP00000432554.1:n.*172A=
ENST00000619430.1:c.349-71A= ENSP00000478572.1:n.349-71A=
NM_000062.2:c.1147A= , LRG_105t1:c.1147A= NP_000053.2:p.Met383=
NM_001032295.1:c.1147A= NP_001027466.1:p.Met383=
NM_000062.3:c.1147A= MANE Select NP_000053.2:p.Met383=
NM_001032295.2:c.1147A= NP_001027466.1:p.Met383=