Canonical Allele Identifier: CA2473780220
Gene: MMACHC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45500443C= , CM000663.2:g.45500443C= GRCh38
NC_000001.10:g.45966115C= , CM000663.1:g.45966115C= GRCh37
NC_000001.9:g.45738702C= NCBI36
NG_013378.1:g.5260C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000401061.9:c.81+30C= MANE Select ENSP00000383840.4:n.81+30C=
ENST00000401061.8:c.81+30C= ENSP00000383840.4:n.81+30C=
ENST00000616135.1:c.-91+30C= ENSP00000478859.1:n.-91+30C=
NM_015506.2:c.81+30C= NP_056321.2:n.81+30C=
XM_005270724.3:c.81+30C= XP_005270781.1:n.81+30C=
XM_011541204.1:c.-142+30C= XP_011539506.1:n.-142+30C=
NM_001330540.1:c.-142+30C= NP_001317469.1:n.-142+30C=
XM_005270724.5:c.81+30C= XP_005270781.1:n.81+30C=
NM_015506.3:c.81+30C= MANE Select NP_056321.2:n.81+30C=
NM_001330540.2:c.-142+30C= NP_001317469.1:n.-142+30C=