Canonical Allele Identifier: CA1337709557
Gene: MLPH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.237554046G= , CM000664.2:g.237554046G= GRCh38
NC_000002.11:g.238462689G= , CM000664.1:g.238462689G= GRCh37
NC_000002.10:g.238127428G= NCBI36
NG_007286.1:g.71760G= , LRG_83:g.71760G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264605.8:c.*454G= MANE Select ENSP00000264605.3:n.*454G=
ENST00000264605.7:c.*454G= ENSP00000264605.3:n.*454G=
NM_001042467.2:c.*454G= NP_001035932.1:n.*454G=
NM_001281473.1:c.*454G= NP_001268402.1:n.*454G=
NM_001281474.1:c.*454G= NP_001268403.1:n.*454G=
NM_024101.6:c.*454G= NP_077006.1:n.*454G=
NR_104019.1:n.2689G=
NM_024101.7:c.*454G= MANE Select NP_077006.1:n.*454G=
NM_001042467.3:c.*454G= NP_001035932.1:n.*454G=
NM_001281473.2:c.*454G= NP_001268402.1:n.*454G=
NM_001281474.2:c.*454G= NP_001268403.1:n.*454G=
NR_104019.2:n.2657G=