Canonical Allele Identifier: CA1297264354
Gene: MMADHC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.149570172A= , CM000664.2:g.149570172A= GRCh38
NC_000002.11:g.150426686A= , CM000664.1:g.150426686A= GRCh37
NC_000002.10:g.150134932A= NCBI36
NG_009189.1:g.22645T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000303319.10:c.697-4T= MANE Select ENSP00000301920.5:n.697-4T=
ENST00000303319.9:c.697-4T= ENSP00000301920.5:n.697-4T=
ENST00000422782.2:c.799-4T= ENSP00000408331.2:n.799-4T=
ENST00000428879.5:c.697-4T= ENSP00000389060.1:n.697-4T=
NM_015702.2:c.697-4T= NP_056517.1:n.697-4T=
NM_015702.3:c.697-4T= MANE Select NP_056517.1:n.697-4T=