Canonical Allele Identifier: CA340131439
Gene: MMACHC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45507396T>G , CM000663.2:g.45507396T>G GRCh38
NC_000001.10:g.45973068T>G , CM000663.1:g.45973068T>G GRCh37
NC_000001.9:g.45745655T>G NCBI36
NG_013378.1:g.12213T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000401061.9:c.122T>G MANE Select ENSP00000383840.4:p.Leu41Arg
ENST00000401061.8:c.122T>G ENSP00000383840.4:p.Leu41Arg
ENST00000616135.1:c.-50T>G ENSP00000478859.1:n.-50T>G
NM_015506.2:c.122T>G NP_056321.2:p.Leu41Arg
XM_005270724.3:c.82-816T>G XP_005270781.1:n.82-816T>G
XM_011541204.1:c.-50T>G XP_011539506.1:n.-50T>G
NM_001330540.1:c.-50T>G NP_001317469.1:n.-50T>G
XM_005270724.5:c.82-816T>G XP_005270781.1:n.82-816T>G
NM_015506.3:c.122T>G MANE Select NP_056321.2:p.Leu41Arg
NM_001330540.2:c.-50T>G NP_001317469.1:n.-50T>G