Canonical Allele Identifier: CA1143757228
Gene: MMACHC HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45500330G= , CM000663.2:g.45500330G= GRCh38
NC_000001.10:g.45966002G= , CM000663.1:g.45966002G= GRCh37
NC_000001.9:g.45738589G= NCBI36
NG_013378.1:g.5147G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000401061.9:c.-3G= MANE Select ENSP00000383840.4:n.-3G=
ENST00000401061.8:c.-3G= ENSP00000383840.4:n.-3G=
NM_015506.2:c.-3G= NP_056321.2:n.-3G=
XM_005270724.3:c.-3G= XP_005270781.1:n.-3G=
XM_011541204.1:c.-225G= XP_011539506.1:n.-225G=
NM_001330540.1:c.-225G= NP_001317469.1:n.-225G=
XM_005270724.5:c.-3G= XP_005270781.1:n.-3G=
NM_015506.3:c.-3G= MANE Select NP_056321.2:n.-3G=
NM_001330540.2:c.-225G= NP_001317469.1:n.-225G=
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