Canonical Allele Identifier: CA360202688

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.79120495A>C , CM000667.2:g.79120495A>C GRCh38
NC_000005.9:g.78416318A>C , CM000667.1:g.78416318A>C GRCh37
NC_000005.8:g.78452074A>C NCBI36
NG_029156.1:g.13715A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000274353.10:c.431A>C (BHMT) MANE Select ENSP00000274353.5:p.Gln144Pro
ENST00000274353.9:c.431A>C (BHMT) ENSP00000274353.5:p.Gln144Pro
ENST00000518707.1:n.279-42T>G (DMGDH)
ENST00000520388.5:n.379-42T>G (DMGDH)
ENST00000523508.1:n.144A>C (BHMT)
ENST00000524080.1:c.166+4596A>C (BHMT) ENSP00000428240.1:n.166+4596A>C
NM_001713.2:c.431A>C (BHMT) NP_001704.2:p.Gln144Pro
NM_001713.3:c.431A>C (BHMT) MANE Select NP_001704.2:p.Gln144Pro