Canonical Allele Identifier: CA1145472384
Gene: MMACHC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45500337A= , CM000663.2:g.45500337A= GRCh38
NC_000001.10:g.45966009A= , CM000663.1:g.45966009A= GRCh37
NC_000001.9:g.45738596A= NCBI36
NG_013378.1:g.5154A=

Transcript Alleles

HGVS Amino-acid change
ENST00000401061.9:c.5A= MANE Select ENSP00000383840.4:p.Glu2=
ENST00000401061.8:c.5A= ENSP00000383840.4:p.Glu2=
NM_015506.2:c.5A= NP_056321.2:p.Glu2=
XM_005270724.3:c.5A= XP_005270781.1:p.Glu2=
XM_011541204.1:c.-218A= XP_011539506.1:n.-218A=
NM_001330540.1:c.-218A= NP_001317469.1:n.-218A=
XM_005270724.5:c.5A= XP_005270781.1:p.Glu2=
NM_015506.3:c.5A= MANE Select NP_056321.2:p.Glu2=
NM_001330540.2:c.-218A= NP_001317469.1:n.-218A=