Canonical Allele Identifier: CA2473780176
Gene: MMACHC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45500335G= , CM000663.2:g.45500335G= GRCh38
NC_000001.10:g.45966007G= , CM000663.1:g.45966007G= GRCh37
NC_000001.9:g.45738594G= NCBI36
NG_013378.1:g.5152G=

Transcript Alleles

HGVS Amino-acid change
ENST00000401061.9:c.3G= MANE Select ENSP00000383840.4:p.Met1=
ENST00000401061.8:c.3G= ENSP00000383840.4:p.Met1=
NM_015506.2:c.3G= NP_056321.2:p.Met1=
XM_005270724.3:c.3G= XP_005270781.1:p.Met1=
XM_011541204.1:c.-220G= XP_011539506.1:n.-220G=
NM_001330540.1:c.-220G= NP_001317469.1:n.-220G=
XM_005270724.5:c.3G= XP_005270781.1:p.Met1=
NM_015506.3:c.3G= MANE Select NP_056321.2:p.Met1=
NM_001330540.2:c.-220G= NP_001317469.1:n.-220G=