Canonical Allele Identifier: CA2535815757
Gene: MMADHC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.149570216A>T , CM000664.2:g.149570216A>T GRCh38
NC_000002.11:g.150426730A>T , CM000664.1:g.150426730A>T GRCh37
NC_000002.10:g.150134976A>T NCBI36
NG_009189.1:g.22601T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000303319.10:c.697-48T>A MANE Select ENSP00000301920.5:n.697-48T>A
ENST00000303319.9:c.697-48T>A ENSP00000301920.5:n.697-48T>A
ENST00000422782.2:c.799-48T>A ENSP00000408331.2:n.799-48T>A
ENST00000428879.5:c.697-48T>A ENSP00000389060.1:n.697-48T>A
NM_015702.2:c.697-48T>A NP_056517.1:n.697-48T>A
NM_015702.3:c.697-48T>A MANE Select NP_056517.1:n.697-48T>A