Canonical Allele Identifier: CA1297264333
Gene: MMADHC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.149570129C= , CM000664.2:g.149570129C= GRCh38
NC_000002.11:g.150426643C= , CM000664.1:g.150426643C= GRCh37
NC_000002.10:g.150134889C= NCBI36
NG_009189.1:g.22688G=

Transcript Alleles

HGVS Amino-acid change
ENST00000303319.10:c.736G= MANE Select ENSP00000301920.5:p.Asp246=
ENST00000303319.9:c.736G= ENSP00000301920.5:p.Asp246=
ENST00000422782.2:c.838G= ENSP00000408331.2:p.Asp280=
ENST00000428879.5:c.736G= ENSP00000389060.1:p.Asp246=
NM_015702.2:c.736G= NP_056517.1:p.Asp246=
NM_015702.3:c.736G= MANE Select NP_056517.1:p.Asp246=