Canonical Allele Identifier: CA1143767108

Gene: MMACHC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45500385C= , CM000663.2:g.45500385C=	GRCh38
NC_000001.10:g.45966057C= , CM000663.1:g.45966057C=	GRCh37
NC_000001.9:g.45738644C=	NCBI36
NG_013378.1:g.5202C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000401061.9:c.53C= MANE Select	ENSP00000383840.4:p.Pro18=
ENST00000401061.8:c.53C=	ENSP00000383840.4:p.Pro18=
ENST00000616135.1:c.-119C=	ENSP00000478859.1:n.-119C=
NM_015506.2:c.53C=	NP_056321.2:p.Pro18=
XM_005270724.3:c.53C=	XP_005270781.1:p.Pro18=
XM_011541204.1:c.-170C=	XP_011539506.1:n.-170C=
NM_001330540.1:c.-170C=	NP_001317469.1:n.-170C=
XM_005270724.5:c.53C=	XP_005270781.1:p.Pro18=
NM_015506.3:c.53C= MANE Select	NP_056321.2:p.Pro18=
NM_001330540.2:c.-170C=	NP_001317469.1:n.-170C=