Canonical Allele Identifier: CA2473783709
Gene: MMACHC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45508923G= , CM000663.2:g.45508923G= GRCh38
NC_000001.10:g.45974595G= , CM000663.1:g.45974595G= GRCh37
NC_000001.9:g.45747182G= NCBI36
NG_013378.1:g.13740G=

Transcript Alleles

HGVS Amino-acid change
ENST00000401061.9:c.557G= MANE Select ENSP00000383840.4:p.Arg186=
ENST00000401061.8:c.557G= ENSP00000383840.4:p.Arg186=
ENST00000616135.1:c.386G= ENSP00000478859.1:p.Arg129=
NM_015506.2:c.557G= NP_056321.2:p.Arg186=
XM_005270724.3:c.362G= XP_005270781.1:p.Arg121=
XM_011541204.1:c.386G= XP_011539506.1:p.Arg129=
NM_001330540.1:c.386G= NP_001317469.1:p.Arg129=
XM_005270724.5:c.362G= XP_005270781.1:p.Arg121=
NM_015506.3:c.557G= MANE Select NP_056321.2:p.Arg186=
NM_001330540.2:c.386G= NP_001317469.1:p.Arg129=