Canonical Allele Identifier: CA2524783638
Gene: MMACHC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45508373G>T , CM000663.2:g.45508373G>T GRCh38
NC_000001.10:g.45974045G>T , CM000663.1:g.45974045G>T GRCh37
NC_000001.9:g.45746632G>T NCBI36
NG_013378.1:g.13190G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000401061.9:c.429+9G>T MANE Select ENSP00000383840.4:n.429+9G>T
ENST00000401061.8:c.429+9G>T ENSP00000383840.4:n.429+9G>T
ENST00000616135.1:c.258+9G>T ENSP00000478859.1:n.258+9G>T
NM_015506.2:c.429+9G>T NP_056321.2:n.429+9G>T
XM_005270724.3:c.234+9G>T XP_005270781.1:n.234+9G>T
XM_011541204.1:c.258+9G>T XP_011539506.1:n.258+9G>T
NM_001330540.1:c.258+9G>T NP_001317469.1:n.258+9G>T
XM_005270724.5:c.234+9G>T XP_005270781.1:n.234+9G>T
NM_015506.3:c.429+9G>T MANE Select NP_056321.2:n.429+9G>T
NM_001330540.2:c.258+9G>T NP_001317469.1:n.258+9G>T