Canonical Allele Identifier: CA1145878555
Gene: MMACHC HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45508643T= , CM000663.2:g.45508643T= GRCh38
NC_000001.10:g.45974315T= , CM000663.1:g.45974315T= GRCh37
NC_000001.9:g.45746902T= NCBI36
NG_013378.1:g.13460T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000401061.9:c.430-153T= MANE Select ENSP00000383840.4:n.430-153T=
ENST00000401061.8:c.430-153T= ENSP00000383840.4:n.430-153T=
ENST00000616135.1:c.259-153T= ENSP00000478859.1:n.259-153T=
NM_015506.2:c.430-153T= NP_056321.2:n.430-153T=
XM_005270724.3:c.235-153T= XP_005270781.1:n.235-153T=
XM_011541204.1:c.259-153T= XP_011539506.1:n.259-153T=
NM_001330540.1:c.259-153T= NP_001317469.1:n.259-153T=
XM_005270724.5:c.235-153T= XP_005270781.1:n.235-153T=
NM_015506.3:c.430-153T= MANE Select NP_056321.2:n.430-153T=
NM_001330540.2:c.259-153T= NP_001317469.1:n.259-153T=
Search 100 bp 5'
Search 100 bp 3'