Canonical Allele Identifier: CA340132197
Gene: MMACHC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45508260C>T , CM000663.2:g.45508260C>T GRCh38
NC_000001.10:g.45973932C>T , CM000663.1:g.45973932C>T GRCh37
NC_000001.9:g.45746519C>T NCBI36
NG_013378.1:g.13077C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000401061.9:c.325C>T MANE Select ENSP00000383840.4:p.Pro109Ser
ENST00000401061.8:c.325C>T ENSP00000383840.4:p.Pro109Ser
ENST00000616135.1:c.154C>T ENSP00000478859.1:p.Pro52Ser
NM_015506.2:c.325C>T NP_056321.2:p.Pro109Ser
XM_005270724.3:c.130C>T XP_005270781.1:p.Pro44Ser
XM_011541204.1:c.154C>T XP_011539506.1:p.Pro52Ser
NM_001330540.1:c.154C>T NP_001317469.1:p.Pro52Ser
XM_005270724.5:c.130C>T XP_005270781.1:p.Pro44Ser
NM_015506.3:c.325C>T MANE Select NP_056321.2:p.Pro109Ser
NM_001330540.2:c.154C>T NP_001317469.1:p.Pro52Ser