Canonical Allele Identifier: CA1337709592
Gene: MLPH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.237554140C= , CM000664.2:g.237554140C= GRCh38
NC_000002.11:g.238462783C= , CM000664.1:g.238462783C= GRCh37
NC_000002.10:g.238127522C= NCBI36
NG_007286.1:g.71854C= , LRG_83:g.71854C=

Transcript Alleles

HGVS Amino-acid change
ENST00000264605.8:c.*548C= MANE Select ENSP00000264605.3:n.*548C=
ENST00000264605.7:c.*548C= ENSP00000264605.3:n.*548C=
NM_001042467.2:c.*548C= NP_001035932.1:n.*548C=
NM_001281473.1:c.*548C= NP_001268402.1:n.*548C=
NM_001281474.1:c.*548C= NP_001268403.1:n.*548C=
NM_024101.6:c.*548C= NP_077006.1:n.*548C=
NR_104019.1:n.2783C=
NM_024101.7:c.*548C= MANE Select NP_077006.1:n.*548C=
NM_001042467.3:c.*548C= NP_001035932.1:n.*548C=
NM_001281473.2:c.*548C= NP_001268402.1:n.*548C=
NM_001281474.2:c.*548C= NP_001268403.1:n.*548C=
NR_104019.2:n.2751C=