Canonical Allele Identifier: CA2473783582
Gene: MMACHC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45508664A= , CM000663.2:g.45508664A= GRCh38
NC_000001.10:g.45974336A= , CM000663.1:g.45974336A= GRCh37
NC_000001.9:g.45746923A= NCBI36
NG_013378.1:g.13481A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000401061.9:c.430-132A= MANE Select ENSP00000383840.4:n.430-132A=
ENST00000401061.8:c.430-132A= ENSP00000383840.4:n.430-132A=
ENST00000616135.1:c.259-132A= ENSP00000478859.1:n.259-132A=
NM_015506.2:c.430-132A= NP_056321.2:n.430-132A=
XM_005270724.3:c.235-132A= XP_005270781.1:n.235-132A=
XM_011541204.1:c.259-132A= XP_011539506.1:n.259-132A=
NM_001330540.1:c.259-132A= NP_001317469.1:n.259-132A=
XM_005270724.5:c.235-132A= XP_005270781.1:n.235-132A=
NM_015506.3:c.430-132A= MANE Select NP_056321.2:n.430-132A=
NM_001330540.2:c.259-132A= NP_001317469.1:n.259-132A=