Canonical Allele Identifier: CA2473783747
Gene: MMACHC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45508977C= , CM000663.2:g.45508977C= GRCh38
NC_000001.10:g.45974649C= , CM000663.1:g.45974649C= GRCh37
NC_000001.9:g.45747236C= NCBI36
NG_013378.1:g.13794C=

Transcript Alleles

HGVS Amino-acid change
ENST00000401061.9:c.611C= MANE Select ENSP00000383840.4:p.Thr204=
ENST00000401061.8:c.611C= ENSP00000383840.4:p.Thr204=
ENST00000616135.1:c.440C= ENSP00000478859.1:p.Thr147=
NM_015506.2:c.611C= NP_056321.2:p.Thr204=
XM_005270724.3:c.416C= XP_005270781.1:p.Thr139=
XM_011541204.1:c.440C= XP_011539506.1:p.Thr147=
NM_001330540.1:c.440C= NP_001317469.1:p.Thr147=
XM_005270724.5:c.416C= XP_005270781.1:p.Thr139=
NM_015506.3:c.611C= MANE Select NP_056321.2:p.Thr204=
NM_001330540.2:c.440C= NP_001317469.1:p.Thr147=