Canonical Allele Identifier: CA2473780179
Gene: MMACHC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45500346T= , CM000663.2:g.45500346T= GRCh38
NC_000001.10:g.45966018T= , CM000663.1:g.45966018T= GRCh37
NC_000001.9:g.45738605T= NCBI36
NG_013378.1:g.5163T=

Transcript Alleles

HGVS Amino-acid change
ENST00000401061.9:c.14T= MANE Select ENSP00000383840.4:p.Val5=
ENST00000401061.8:c.14T= ENSP00000383840.4:p.Val5=
ENST00000616135.1:c.-158T= ENSP00000478859.1:n.-158T=
NM_015506.2:c.14T= NP_056321.2:p.Val5=
XM_005270724.3:c.14T= XP_005270781.1:p.Val5=
XM_011541204.1:c.-209T= XP_011539506.1:n.-209T=
NM_001330540.1:c.-209T= NP_001317469.1:n.-209T=
XM_005270724.5:c.14T= XP_005270781.1:p.Val5=
NM_015506.3:c.14T= MANE Select NP_056321.2:p.Val5=
NM_001330540.2:c.-209T= NP_001317469.1:n.-209T=