Canonical Allele Identifier: CA2473783027
Gene: MMACHC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45507397A= , CM000663.2:g.45507397A= GRCh38
NC_000001.10:g.45973069A= , CM000663.1:g.45973069A= GRCh37
NC_000001.9:g.45745656A= NCBI36
NG_013378.1:g.12214A=

Transcript Alleles

HGVS Amino-acid change
ENST00000401061.9:c.123A= MANE Select ENSP00000383840.4:p.Leu41=
ENST00000401061.8:c.123A= ENSP00000383840.4:p.Leu41=
ENST00000616135.1:c.-49A= ENSP00000478859.1:n.-49A=
NM_015506.2:c.123A= NP_056321.2:p.Leu41=
XM_005270724.3:c.82-815A= XP_005270781.1:n.82-815A=
XM_011541204.1:c.-49A= XP_011539506.1:n.-49A=
NM_001330540.1:c.-49A= NP_001317469.1:n.-49A=
XM_005270724.5:c.82-815A= XP_005270781.1:n.82-815A=
NM_015506.3:c.123A= MANE Select NP_056321.2:p.Leu41=
NM_001330540.2:c.-49A= NP_001317469.1:n.-49A=