Canonical Allele Identifier: CA1327644378
Gene: MREG HGNC NCBI
PECR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216033927T= , CM000664.2:g.216033927T= GRCh38
NC_000002.11:g.216898650T= , CM000664.1:g.216898650T= GRCh37
NC_000002.10:g.216606895T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000424992.5:c.-68+35A= (MREG) ENSP00000413302.1:n.-68+35A=
ENST00000442122.5:c.*440+5264A= (PECR) ENSP00000395512.1:n.*440+5264A=
XR_001738847.2:n.1056-1075A= (PECR)
NM_001372189.1:c.-68+35A= (MREG) NP_001359118.1:n.-68+35A=
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