Canonical Allele Identifier: CA1557735761

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.79120620_79120621delinsTG , CM000667.2:g.79120620_79120621delinsTG GRCh38
NC_000005.9:g.78416443_78416444delinsTG , CM000667.1:g.78416443_78416444delinsTG GRCh37
NC_000005.8:g.78452199_78452200delinsTG NCBI36
NG_029156.1:g.13840_13841delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000274353.10:c.477+79_477+80delinsTG (BHMT) MANE Select ENSP00000274353.5:n.477+79_477+80delinsTG...
ENST00000274353.9:c.477+79_477+80delinsTG (BHMT) ENSP00000274353.5:n.477+79_477+80delinsTG...
ENST00000518707.1:n.279-168_279-167delinsCA (DMGDH)
ENST00000520388.5:n.379-168_379-167delinsCA (DMGDH)
ENST00000523508.1:n.190+79_190+80delinsTG (BHMT)
ENST00000524080.1:c.166+4721_166+4722delinsTG (BHMT) ENSP00000428240.1:n.166+4721_166+4722deli...
NM_001713.2:c.477+79_477+80delinsTG (BHMT) NP_001704.2:n.477+79_477+80delinsTG
NM_001713.3:c.477+79_477+80delinsTG (BHMT) MANE Select NP_001704.2:n.477+79_477+80delinsTG