Canonical Allele Identifier: CA2473780178
Gene: MMACHC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45500343A= , CM000663.2:g.45500343A= GRCh38
NC_000001.10:g.45966015A= , CM000663.1:g.45966015A= GRCh37
NC_000001.9:g.45738602A= NCBI36
NG_013378.1:g.5160A=

Transcript Alleles

HGVS Amino-acid change
ENST00000401061.9:c.11A= MANE Select ENSP00000383840.4:p.Lys4=
ENST00000401061.8:c.11A= ENSP00000383840.4:p.Lys4=
ENST00000616135.1:c.-161A= ENSP00000478859.1:n.-161A=
NM_015506.2:c.11A= NP_056321.2:p.Lys4=
XM_005270724.3:c.11A= XP_005270781.1:p.Lys4=
XM_011541204.1:c.-212A= XP_011539506.1:n.-212A=
NM_001330540.1:c.-212A= NP_001317469.1:n.-212A=
XM_005270724.5:c.11A= XP_005270781.1:p.Lys4=
NM_015506.3:c.11A= MANE Select NP_056321.2:p.Lys4=
NM_001330540.2:c.-212A= NP_001317469.1:n.-212A=