Canonical Allele Identifier: CA2473783715

Gene: MMACHC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45508935T= , CM000663.2:g.45508935T=	GRCh38
NC_000001.10:g.45974607T= , CM000663.1:g.45974607T=	GRCh37
NC_000001.9:g.45747194T=	NCBI36
NG_013378.1:g.13752T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000401061.9:c.569T= MANE Select	ENSP00000383840.4:p.Ile190=
ENST00000401061.8:c.569T=	ENSP00000383840.4:p.Ile190=
ENST00000616135.1:c.398T=	ENSP00000478859.1:p.Ile133=
NM_015506.2:c.569T=	NP_056321.2:p.Ile190=
XM_005270724.3:c.374T=	XP_005270781.1:p.Ile125=
XM_011541204.1:c.398T=	XP_011539506.1:p.Ile133=
NM_001330540.1:c.398T=	NP_001317469.1:p.Ile133=
XM_005270724.5:c.374T=	XP_005270781.1:p.Ile125=
NM_015506.3:c.569T= MANE Select	NP_056321.2:p.Ile190=
NM_001330540.2:c.398T=	NP_001317469.1:p.Ile133=