Canonical Allele Identifier: CA1297264228
Gene: MMADHC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.149569906C= , CM000664.2:g.149569906C= GRCh38
NC_000002.11:g.150426420C= , CM000664.1:g.150426420C= GRCh37
NC_000002.10:g.150134666C= NCBI36
NG_009189.1:g.22911G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000303319.10:c.*68G= MANE Select ENSP00000301920.5:n.*68G=
ENST00000303319.9:c.*68G= ENSP00000301920.5:n.*68G=
ENST00000422782.2:c.*68G= ENSP00000408331.2:n.*68G=
ENST00000428879.5:c.*68G= ENSP00000389060.1:n.*68G=
NM_015702.2:c.*68G= NP_056517.1:n.*68G=
NM_015702.3:c.*68G= MANE Select NP_056517.1:n.*68G=