Canonical Allele Identifier: CA2473783300
Gene: MMACHC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45508109G= , CM000663.2:g.45508109G= GRCh38
NC_000001.10:g.45973781G= , CM000663.1:g.45973781G= GRCh37
NC_000001.9:g.45746368G= NCBI36
NG_013378.1:g.12926G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000401061.9:c.277-103G= MANE Select ENSP00000383840.4:n.277-103G=
ENST00000401061.8:c.277-103G= ENSP00000383840.4:n.277-103G=
ENST00000616135.1:c.106-103G= ENSP00000478859.1:n.106-103G=
NM_015506.2:c.277-103G= NP_056321.2:n.277-103G=
XM_005270724.3:c.82-103G= XP_005270781.1:n.82-103G=
XM_011541204.1:c.106-103G= XP_011539506.1:n.106-103G=
NM_001330540.1:c.106-103G= NP_001317469.1:n.106-103G=
XM_005270724.5:c.82-103G= XP_005270781.1:n.82-103G=
NM_015506.3:c.277-103G= MANE Select NP_056321.2:n.277-103G=
NM_001330540.2:c.106-103G= NP_001317469.1:n.106-103G=