Canonical Allele Identifier: CA360201938

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.79120410G>C , CM000667.2:g.79120410G>C GRCh38
NC_000005.9:g.78416233G>C , CM000667.1:g.78416233G>C GRCh37
NC_000005.8:g.78451989G>C NCBI36
NG_029156.1:g.13630G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000274353.10:c.346G>C (BHMT) MANE Select ENSP00000274353.5:p.Ala116Pro
ENST00000274353.9:c.346G>C (BHMT) ENSP00000274353.5:p.Ala116Pro
ENST00000518707.1:n.322C>G (DMGDH)
ENST00000520388.5:n.422C>G (DMGDH)
ENST00000523508.1:n.59G>C (BHMT)
ENST00000524080.1:c.166+4511G>C (BHMT) ENSP00000428240.1:n.166+4511G>C
NM_001713.2:c.346G>C (BHMT) NP_001704.2:p.Ala116Pro
NM_001713.3:c.346G>C (BHMT) MANE Select NP_001704.2:p.Ala116Pro