Canonical Allele Identifier: CA1557732019

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.79114790_79114791delinsTG , CM000667.2:g.79114790_79114791delinsTG GRCh38
NC_000005.9:g.78410613_78410614delinsTG , CM000667.1:g.78410613_78410614delinsTG GRCh37
NC_000005.8:g.78446369_78446370delinsTG NCBI36
NG_029156.1:g.8010_8011delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000274353.10:c.34-977_34-976delinsTG (BHMT) MANE Select ENSP00000274353.5:n.34-977_34-976delinsTG...
ENST00000274353.9:c.34-977_34-976delinsTG (BHMT) ENSP00000274353.5:n.34-977_34-976delinsTG...
ENST00000520335.5:n.111-977_111-976delinsTG (BHMT)
ENST00000520388.5:n.491+5550_491+5551delinsCA (DMGDH)
ENST00000520703.1:n.111-977_111-976delinsTG (BHMT)
ENST00000524080.1:c.34-977_34-976delinsTG (BHMT) ENSP00000428240.1:n.34-977_34-976delinsTG...
NM_001713.2:c.34-977_34-976delinsTG (BHMT) NP_001704.2:n.34-977_34-976delinsTG
NM_001713.3:c.34-977_34-976delinsTG (BHMT) MANE Select NP_001704.2:n.34-977_34-976delinsTG