Canonical Allele Identifier: CA1975539445
Gene: SERPING1 HGNC NCBI

Linked Data

dbSNP Id: rs1945519592

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57614650_57614652dup , CM000673.2:g.57614650_57614652dup GRCh38
NC_000011.9:g.57382123_57382125dup , CM000673.1:g.57382123_57382125dup GRCh37
NC_000011.8:g.57138699_57138701dup NCBI36
NG_009625.1:g.22097_22099dup , LRG_105:g.22097_22099dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.*69_*71dup MANE Select ENSP00000278407.4:n.*69_*71dup
ENST00000528996.2:c.*469_*471dup ENSP00000431226.2:n.*469_*471dup
ENST00000531605.2:c.*1348_*1350dup ENSP00000503752.1:n.*1348_*1350dup
ENST00000619430.2:c.*69_*71dup ENSP00000478572.2:n.*69_*71dup
ENST00000676670.1:c.*15+54_*15+56dup ENSP00000504807.1:n.*15+54_*15+56dup
ENST00000676741.1:n.2654_2656dup
ENST00000677624.1:c.*992_*994dup ENSP00000503979.1:n.*992_*994dup
ENST00000677625.1:c.*69_*71dup ENSP00000502857.1:n.*69_*71dup
ENST00000677856.1:n.1825_1827dup
ENST00000677915.1:c.*469_*471dup ENSP00000503118.1:n.*469_*471dup
ENST00000678533.1:c.*1072+54_*1072+56dup ENSP00000503873.1:n.*1072+54_*1072+56dup
ENST00000678592.1:c.*512_*514dup ENSP00000504424.1:n.*512_*514dup
ENST00000278407.8:c.*69_*71dup ENSP00000278407.4:n.*69_*71dup
ENST00000340687.10:c.*69_*71dup ENSP00000341861.6:n.*69_*71dup
ENST00000378323.8:c.*69_*71dup ENSP00000367574.4:n.*69_*71dup
ENST00000378324.6:c.*69_*71dup ENSP00000367575.2:n.*69_*71dup
ENST00000403558.1:c.*69_*71dup ENSP00000384420.1:n.*69_*71dup
ENST00000528996.1:c.773_775dup ENSP00000431226.1:n.773_775dup
ENST00000531797.5:c.*597_*599dup ENSP00000432554.1:n.*597_*599dup
NM_000062.2:c.*69_*71dup , LRG_105t1:c.*69_*71dup NP_000053.2:n.*69_*71dup
NM_001032295.1:c.*69_*71dup NP_001027466.1:n.*69_*71dup
NM_000062.3:c.*69_*71dup MANE Select NP_000053.2:n.*69_*71dup
NM_001032295.2:c.*69_*71dup NP_001027466.1:n.*69_*71dup