Canonical Allele Identifier: CA2473783780
Gene: MMACHC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45509031_45509034delinsACTT , CM000663.2:g.45509031_45509034delinsACTT GRCh38
NC_000001.10:g.45974703_45974706delinsACTT , CM000663.1:g.45974703_45974706delinsACTT GRCh37
NC_000001.9:g.45747290_45747293delinsACTT NCBI36
NG_013378.1:g.13848_13851delinsACTT

Transcript Alleles

HGVS Amino-acid change
ENST00000401061.9:c.665_668delinsACTT MANE Select ENSP00000383840.4:p.Tyr222=
ENST00000401061.8:c.665_668delinsACTT ENSP00000383840.4:p.Tyr222=
ENST00000616135.1:c.494_497delinsACTT ENSP00000478859.1:p.Tyr165=
NM_015506.2:c.665_668delinsACTT NP_056321.2:p.Tyr222=
XM_005270724.3:c.470_473delinsACTT XP_005270781.1:p.Tyr157=
XM_011541204.1:c.494_497delinsACTT XP_011539506.1:p.Tyr165=
NM_001330540.1:c.494_497delinsACTT NP_001317469.1:p.Tyr165=
XM_005270724.5:c.470_473delinsACTT XP_005270781.1:p.Tyr157=
NM_015506.3:c.665_668delinsACTT MANE Select NP_056321.2:p.Tyr222=
NM_001330540.2:c.494_497delinsACTT NP_001317469.1:p.Tyr165=