Canonical Allele Identifier: CA1327642250
Gene: MREG HGNC NCBI
PECR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216028785T= , CM000664.2:g.216028785T= GRCh38
NC_000002.11:g.216893508T= , CM000664.1:g.216893508T= GRCh37
NC_000002.10:g.216601753T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000420348.1:c.-68+4004A= (MREG) ENSP00000404470.1:n.-68+4004A=
ENST00000424992.5:c.-68+5177A= (MREG) ENSP00000413302.1:n.-68+5177A=
ENST00000439791.5:c.-68+4898A= (MREG) ENSP00000411076.1:n.-68+4898A=
ENST00000442122.5:c.*440+10406A= (PECR) ENSP00000395512.1:n.*440+10406A=
NM_001372189.1:c.-68+5177A= (MREG) NP_001359118.1:n.-68+5177A=
NM_001372190.1:c.-68+4898A= (MREG) NP_001359119.1:n.-68+4898A=
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