Canonical Allele Identifier: CA1327642258
Gene: MREG HGNC NCBI
PECR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216028802A= , CM000664.2:g.216028802A= GRCh38
NC_000002.11:g.216893525A= , CM000664.1:g.216893525A= GRCh37
NC_000002.10:g.216601770A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000420348.1:c.-68+3987T= (MREG) ENSP00000404470.1:n.-68+3987T=
ENST00000424992.5:c.-68+5160T= (MREG) ENSP00000413302.1:n.-68+5160T=
ENST00000439791.5:c.-68+4881T= (MREG) ENSP00000411076.1:n.-68+4881T=
ENST00000442122.5:c.*440+10389T= (PECR) ENSP00000395512.1:n.*440+10389T=
NM_001372189.1:c.-68+5160T= (MREG) NP_001359118.1:n.-68+5160T=
NM_001372190.1:c.-68+4881T= (MREG) NP_001359119.1:n.-68+4881T=
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