Canonical Allele Identifier: CA1297264347

Gene: MMADHC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.149570160T= , CM000664.2:g.149570160T=	GRCh38
NC_000002.11:g.150426674T= , CM000664.1:g.150426674T=	GRCh37
NC_000002.10:g.150134920T=	NCBI36
NG_009189.1:g.22657A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303319.10:c.705A= MANE Select	ENSP00000301920.5:p.Gly235=
ENST00000303319.9:c.705A=	ENSP00000301920.5:p.Gly235=
ENST00000422782.2:c.807A=	ENSP00000408331.2:p.Gly269=
ENST00000428879.5:c.705A=	ENSP00000389060.1:p.Gly235=
NM_015702.2:c.705A=	NP_056517.1:p.Gly235=
NM_015702.3:c.705A= MANE Select	NP_056517.1:p.Gly235=