Canonical Allele Identifier: CA1297264140
Gene: MMADHC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.149569652T= , CM000664.2:g.149569652T= GRCh38
NC_000002.11:g.150426166T= , CM000664.1:g.150426166T= GRCh37
NC_000002.10:g.150134412T= NCBI36
NG_009189.1:g.23165A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000303319.10:c.*322A= MANE Select ENSP00000301920.5:n.*322A=
ENST00000303319.9:c.*322A= ENSP00000301920.5:n.*322A=
ENST00000428879.5:c.*322A= ENSP00000389060.1:n.*322A=
NM_015702.2:c.*322A= NP_056517.1:n.*322A=
NM_015702.3:c.*322A= MANE Select NP_056517.1:n.*322A=