Canonical Allele Identifier: CA2743432335
Gene: MMACHC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45508677_45508679del , CM000663.2:g.45508677_45508679del GRCh38
NC_000001.10:g.45974349_45974351del , CM000663.1:g.45974349_45974351del GRCh37
NC_000001.9:g.45746936_45746938del NCBI36
NG_013378.1:g.13494_13496del

Transcript Alleles

HGVS Amino-acid Change
ENST00000401061.9:c.430-119_430-117del MANE Select ENSP00000383840.4:n.430-119_430-117del
ENST00000401061.8:c.430-119_430-117del ENSP00000383840.4:n.430-119_430-117del
ENST00000616135.1:c.259-119_259-117del ENSP00000478859.1:n.259-119_259-117del
NM_015506.2:c.430-119_430-117del NP_056321.2:n.430-119_430-117del
XM_005270724.3:c.235-119_235-117del XP_005270781.1:n.235-119_235-117del
XM_011541204.1:c.259-119_259-117del XP_011539506.1:n.259-119_259-117del
NM_001330540.1:c.259-119_259-117del NP_001317469.1:n.259-119_259-117del
XM_005270724.5:c.235-119_235-117del XP_005270781.1:n.235-119_235-117del
NM_015506.3:c.430-119_430-117del MANE Select NP_056321.2:n.430-119_430-117del
NM_001330540.2:c.259-119_259-117del NP_001317469.1:n.259-119_259-117del