Canonical Allele Identifier: CA340133465
Gene: MMACHC HGNC NCBI

Linked Data

gnomAD v4: 1-45508929-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45508929A>T , CM000663.2:g.45508929A>T GRCh38
NC_000001.10:g.45974601A>T , CM000663.1:g.45974601A>T GRCh37
NC_000001.9:g.45747188A>T NCBI36
NG_013378.1:g.13746A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000401061.9:c.563A>T MANE Select ENSP00000383840.4:p.Asp188Val
ENST00000401061.8:c.563A>T ENSP00000383840.4:p.Asp188Val
ENST00000616135.1:c.392A>T ENSP00000478859.1:p.Asp131Val
NM_015506.2:c.563A>T NP_056321.2:p.Asp188Val
XM_005270724.3:c.368A>T XP_005270781.1:p.Asp123Val
XM_011541204.1:c.392A>T XP_011539506.1:p.Asp131Val
NM_001330540.1:c.392A>T NP_001317469.1:p.Asp131Val
XM_005270724.5:c.368A>T XP_005270781.1:p.Asp123Val
NM_015506.3:c.563A>T MANE Select NP_056321.2:p.Asp188Val
NM_001330540.2:c.392A>T NP_001317469.1:p.Asp131Val