Canonical Allele Identifier: CA380695714
Gene: SERPING1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.57367850G>C (hg19) chr11:g.57600377G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57600377G>C , CM000673.2:g.57600377G>C GRCh38
NC_000011.9:g.57367850G>C , CM000673.1:g.57367850G>C GRCh37
NC_000011.8:g.57124426G>C NCBI36
NG_009625.1:g.7824G>C , LRG_105:g.7824G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000278407.9:c.550G>C MANE Select ENSP00000278407.4:p.Gly184Arg
ENST00000528996.2:c.58+2049G>C ENSP00000431226.2:n.58+2049G>C
ENST00000531605.2:c.52-1658G>C ENSP00000503752.1:n.52-1658G>C
ENST00000619430.2:c.550G>C ENSP00000478572.2:p.Gly184Arg
ENST00000676670.1:c.550G>C ENSP00000504807.1:p.Gly184Arg
ENST00000676741.1:n.1632G>C
ENST00000677275.1:n.537G>C
ENST00000677624.1:c.550G>C ENSP00000503979.1:p.Gly184Arg
ENST00000677625.1:c.550G>C ENSP00000502857.1:p.Gly184Arg
ENST00000677856.1:n.609G>C
ENST00000677915.1:c.550G>C ENSP00000503118.1:p.Gly184Arg
ENST00000678533.1:c.52-1658G>C ENSP00000503873.1:n.52-1658G>C
ENST00000678592.1:c.550G>C ENSP00000504424.1:p.Gly184Arg
ENST00000278407.8:c.550G>C ENSP00000278407.4:p.Gly184Arg
ENST00000340687.10:c.550G>C ENSP00000341861.6:p.Gly184Arg
ENST00000378323.8:c.565G>C ENSP00000367574.4:p.Gly189Arg
ENST00000378324.6:c.394G>C ENSP00000367575.2:p.Gly132Arg
ENST00000403558.1:c.652G>C ENSP00000384420.1:p.Gly218Arg
ENST00000531133.5:c.52-1658G>C ENSP00000435431.1:n.52-1658G>C
ENST00000531797.5:c.52-1658G>C ENSP00000432554.1:n.52-1658G>C
ENST00000619430.1:c.348+202G>C ENSP00000478572.1:n.348+202G>C
NM_000062.2:c.550G>C , LRG_105t1:c.550G>C NP_000053.2:p.Gly184Arg
NM_001032295.1:c.550G>C NP_001027466.1:p.Gly184Arg
NM_000062.3:c.550G>C MANE Select NP_000053.2:p.Gly184Arg
NM_001032295.2:c.550G>C NP_001027466.1:p.Gly184Arg
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