Canonical Allele Identifier: CA1337709602

Gene: MLPH

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237554156C= , CM000664.2:g.237554156C=	GRCh38
NC_000002.11:g.238462799C= , CM000664.1:g.238462799C=	GRCh37
NC_000002.10:g.238127538C=	NCBI36
NG_007286.1:g.71870C= , LRG_83:g.71870C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264605.8:c.*564C= MANE Select	ENSP00000264605.3:n.*564C=
ENST00000264605.7:c.*564C=	ENSP00000264605.3:n.*564C=
NM_001042467.2:c.*564C=	NP_001035932.1:n.*564C=
NM_001281473.1:c.*564C=	NP_001268402.1:n.*564C=
NM_001281474.1:c.*564C=	NP_001268403.1:n.*564C=
NM_024101.6:c.*564C=	NP_077006.1:n.*564C=
NR_104019.1:n.2799C=
NM_024101.7:c.*564C= MANE Select	NP_077006.1:n.*564C=
NM_001042467.3:c.*564C=	NP_001035932.1:n.*564C=
NM_001281473.2:c.*564C=	NP_001268402.1:n.*564C=
NM_001281474.2:c.*564C=	NP_001268403.1:n.*564C=
NR_104019.2:n.2767C=