Canonical Allele Identifier: CA2473783723
Gene: MMACHC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45508941T= , CM000663.2:g.45508941T= GRCh38
NC_000001.10:g.45974613T= , CM000663.1:g.45974613T= GRCh37
NC_000001.9:g.45747200T= NCBI36
NG_013378.1:g.13758T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000401061.9:c.575T= MANE Select ENSP00000383840.4:p.Leu192=
ENST00000401061.8:c.575T= ENSP00000383840.4:p.Leu192=
ENST00000616135.1:c.404T= ENSP00000478859.1:p.Leu135=
NM_015506.2:c.575T= NP_056321.2:p.Leu192=
XM_005270724.3:c.380T= XP_005270781.1:p.Leu127=
XM_011541204.1:c.404T= XP_011539506.1:p.Leu135=
NM_001330540.1:c.404T= NP_001317469.1:p.Leu135=
XM_005270724.5:c.380T= XP_005270781.1:p.Leu127=
NM_015506.3:c.575T= MANE Select NP_056321.2:p.Leu192=
NM_001330540.2:c.404T= NP_001317469.1:p.Leu135=