Canonical Allele Identifier: CA417704722

Gene: MMACHC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45507529C>T , CM000663.2:g.45507529C>T	GRCh38
NC_000001.10:g.45973201C>T , CM000663.1:g.45973201C>T	GRCh37
NC_000001.9:g.45745788C>T	NCBI36
NG_013378.1:g.12346C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000401061.9:c.255C>T MANE Select	ENSP00000383840.4:p.Tyr85=
ENST00000401061.8:c.255C>T	ENSP00000383840.4:p.Tyr85=
ENST00000616135.1:c.84C>T	ENSP00000478859.1:p.Tyr28=
NM_015506.2:c.255C>T	NP_056321.2:p.Tyr85=
XM_005270724.3:c.82-683C>T	XP_005270781.1:n.82-683C>T
XM_011541204.1:c.84C>T	XP_011539506.1:p.Tyr28=
NM_001330540.1:c.84C>T	NP_001317469.1:p.Tyr28=
XM_005270724.5:c.82-683C>T	XP_005270781.1:n.82-683C>T
NM_015506.3:c.255C>T MANE Select	NP_056321.2:p.Tyr85=
NM_001330540.2:c.84C>T	NP_001317469.1:p.Tyr28=