Canonical Allele Identifier: CA340133171
Community Standard Title: NM_015506.3(MMACHC):c.482G>T (p.Arg161Leu)
Gene: MMACHC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45508848G>T , CM000663.2:g.45508848G>T GRCh38
NC_000001.10:g.45974520G>T , CM000663.1:g.45974520G>T GRCh37
NC_000001.9:g.45747107G>T NCBI36
NG_013378.1:g.13665G>T

Transcript Alleles

HGVS Amino-acid Change
NM_015506.3:c.482G>T MANE Select NP_056321.2:p.Arg161Leu
ENST00000401061.9:c.482G>T MANE Select ENSP00000383840.4:p.Arg161Leu
NM_001330540.1:c.311G>T NP_001317469.1:p.Arg104Leu
NM_001330540.2:c.311G>T NP_001317469.1:p.Arg104Leu
NM_015506.2:c.482G>T NP_056321.2:p.Arg161Leu
ENST00000401061.8:c.482G>T ENSP00000383840.4:p.Arg161Leu
ENST00000616135.1:c.311G>T ENSP00000478859.1:p.Arg104Leu
XM_005270724.3:c.287G>T XP_005270781.1:p.Arg96Leu
XM_005270724.5:c.287G>T XP_005270781.1:p.Arg96Leu
XM_011541204.1:c.311G>T XP_011539506.1:p.Arg104Leu