Canonical Allele Identifier: CA913075178
Gene: MMACHC HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.45974604dup (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45508932dup , CM000663.2:g.45508932dup GRCh38
NC_000001.10:g.45974604dup , CM000663.1:g.45974604dup GRCh37
NC_000001.9:g.45747191dup NCBI36
NG_013378.1:g.13749dup

Transcript Alleles

HGVS Amino-acid change
ENST00000401061.9:c.566dup MANE Select ENSP00000383840.4:p.Ile190TyrfsTer13
ENST00000401061.8:c.566dup ENSP00000383840.4:p.Ile190TyrfsTer13
ENST00000616135.1:c.395dup ENSP00000478859.1:p.Ile133TyrfsTer13
NM_015506.2:c.566dup NP_056321.2:p.Ile190TyrfsTer13
XM_005270724.3:c.371dup XP_005270781.1:p.Ile125TyrfsTer13
XM_011541204.1:c.395dup XP_011539506.1:p.Ile133TyrfsTer13
NM_001330540.1:c.395dup NP_001317469.1:p.Ile133TyrfsTer13
XM_005270724.5:c.371dup XP_005270781.1:p.Ile125TyrfsTer13
NM_015506.3:c.566dup MANE Select NP_056321.2:p.Ile190TyrfsTer13
NM_001330540.2:c.395dup NP_001317469.1:p.Ile133TyrfsTer13