Canonical Allele Identifier: CA1327642327
Gene: MREG HGNC NCBI
PECR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216028978T= , CM000664.2:g.216028978T= GRCh38
NC_000002.11:g.216893701T= , CM000664.1:g.216893701T= GRCh37
NC_000002.10:g.216601946T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000420348.1:c.-68+3811A= (MREG) ENSP00000404470.1:n.-68+3811A=
ENST00000424992.5:c.-68+4984A= (MREG) ENSP00000413302.1:n.-68+4984A=
ENST00000439791.5:c.-68+4705A= (MREG) ENSP00000411076.1:n.-68+4705A=
ENST00000442122.5:c.*440+10213A= (PECR) ENSP00000395512.1:n.*440+10213A=
NM_001372189.1:c.-68+4984A= (MREG) NP_001359118.1:n.-68+4984A=
NM_001372190.1:c.-68+4705A= (MREG) NP_001359119.1:n.-68+4705A=
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