Canonical Allele Identifier: CA340133447
Gene: MMACHC HGNC NCBI

Linked Data

gnomAD v4: 1-45508925-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45508925G>C , CM000663.2:g.45508925G>C GRCh38
NC_000001.10:g.45974597G>C , CM000663.1:g.45974597G>C GRCh37
NC_000001.9:g.45747184G>C NCBI36
NG_013378.1:g.13742G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000401061.9:c.559G>C MANE Select ENSP00000383840.4:p.Ala187Pro
ENST00000401061.8:c.559G>C ENSP00000383840.4:p.Ala187Pro
ENST00000616135.1:c.388G>C ENSP00000478859.1:p.Ala130Pro
NM_015506.2:c.559G>C NP_056321.2:p.Ala187Pro
XM_005270724.3:c.364G>C XP_005270781.1:p.Ala122Pro
XM_011541204.1:c.388G>C XP_011539506.1:p.Ala130Pro
NM_001330540.1:c.388G>C NP_001317469.1:p.Ala130Pro
XM_005270724.5:c.364G>C XP_005270781.1:p.Ala122Pro
NM_015506.3:c.559G>C MANE Select NP_056321.2:p.Ala187Pro
NM_001330540.2:c.388G>C NP_001317469.1:p.Ala130Pro