Canonical Allele Identifier: CA1297264170
Gene: MMADHC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.149569734G= , CM000664.2:g.149569734G= GRCh38
NC_000002.11:g.150426248G= , CM000664.1:g.150426248G= GRCh37
NC_000002.10:g.150134494G= NCBI36
NG_009189.1:g.23083C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000303319.10:c.*240C= MANE Select ENSP00000301920.5:n.*240C=
ENST00000303319.9:c.*240C= ENSP00000301920.5:n.*240C=
ENST00000422782.2:c.*240C= ENSP00000408331.2:n.*240C=
ENST00000428879.5:c.*240C= ENSP00000389060.1:n.*240C=
NM_015702.2:c.*240C= NP_056517.1:n.*240C=
NM_015702.3:c.*240C= MANE Select NP_056517.1:n.*240C=