Canonical Allele Identifier: CA348869436
Gene: MMADHC HGNC NCBI

Linked Data

COSMIC: COSM88097

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.149570152G>C , CM000664.2:g.149570152G>C GRCh38
NC_000002.11:g.150426666G>C , CM000664.1:g.150426666G>C GRCh37
NC_000002.10:g.150134912G>C NCBI36
NG_009189.1:g.22665C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000303319.10:c.713C>G MANE Select ENSP00000301920.5:p.Thr238Arg
ENST00000303319.9:c.713C>G ENSP00000301920.5:p.Thr238Arg
ENST00000422782.2:c.815C>G ENSP00000408331.2:p.Thr272Arg
ENST00000428879.5:c.713C>G ENSP00000389060.1:p.Thr238Arg
NM_015702.2:c.713C>G NP_056517.1:p.Thr238Arg
NM_015702.3:c.713C>G MANE Select NP_056517.1:p.Thr238Arg