Canonical Allele Identifier: CA340133434
Gene: MMACHC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45508922A>T , CM000663.2:g.45508922A>T GRCh38
NC_000001.10:g.45974594A>T , CM000663.1:g.45974594A>T GRCh37
NC_000001.9:g.45747181A>T NCBI36
NG_013378.1:g.13739A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000401061.9:c.556A>T MANE Select ENSP00000383840.4:p.Arg186Ter
ENST00000401061.8:c.556A>T ENSP00000383840.4:p.Arg186Ter
ENST00000616135.1:c.385A>T ENSP00000478859.1:p.Arg129Ter
NM_015506.2:c.556A>T NP_056321.2:p.Arg186Ter
XM_005270724.3:c.361A>T XP_005270781.1:p.Arg121Ter
XM_011541204.1:c.385A>T XP_011539506.1:p.Arg129Ter
NM_001330540.1:c.385A>T NP_001317469.1:p.Arg129Ter
XM_005270724.5:c.361A>T XP_005270781.1:p.Arg121Ter
NM_015506.3:c.556A>T MANE Select NP_056321.2:p.Arg186Ter
NM_001330540.2:c.385A>T NP_001317469.1:p.Arg129Ter