Canonical Allele Identifier: CA1337695115

Gene: MLPH

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237527391A= , CM000664.2:g.237527391A=	GRCh38
NC_000002.11:g.238436034A= , CM000664.1:g.238436034A=	GRCh37
NC_000002.10:g.238100773A=	NCBI36
NG_007286.1:g.45105A= , LRG_83:g.45105A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264605.8:c.895A= MANE Select	ENSP00000264605.3:p.Arg299=
ENST00000264605.7:c.895A=	ENSP00000264605.3:p.Arg299=
ENST00000338530.8:c.895A=	ENSP00000341845.4:p.Arg299=
ENST00000409373.5:c.775A=	ENSP00000386780.1:p.Arg259=
ENST00000410032.5:c.675+7362A=	ENSP00000386338.1:n.675+7362A=
ENST00000436965.5:c.141A=
ENST00000437893.5:c.300+1586A=	ENSP00000412438.1:n.300+1586A=
ENST00000464123.5:n.960A=
ENST00000468178.5:n.1106A=
ENST00000478712.5:n.574A=
ENST00000482528.1:n.147A=
ENST00000485956.1:n.271A=
ENST00000494110.5:n.575A=
ENST00000495439.5:n.1272A=
NM_001042467.2:c.895A=	NP_001035932.1:p.Arg299=
NM_001281473.1:c.775A=	NP_001268402.1:p.Arg259=
NM_001281474.1:c.675+7362A=	NP_001268403.1:n.675+7362A=
NM_024101.6:c.895A=	NP_077006.1:p.Arg299=
NR_104019.1:n.1138A=
XM_006712737.1:c.775A=	XP_006712800.1:p.Arg259=
XM_006712739.1:c.895A=	XP_006712802.1:p.Arg299=
XM_006712740.1:c.775A=	XP_006712803.1:p.Arg259=
XM_011511811.1:c.895A=	XP_011510113.1:p.Arg299=
XM_011511812.1:c.460A=	XP_011510114.1:p.Arg154=
XR_923025.1:n.1106A=
XM_017004893.1:c.895A=	XP_016860382.1:p.Arg299=
XM_017004894.2:c.895A=	XP_016860383.1:p.Arg299=
NM_024101.7:c.895A= MANE Select	NP_077006.1:p.Arg299=
NM_001042467.3:c.895A=	NP_001035932.1:p.Arg299=
NM_001281473.2:c.775A=	NP_001268402.1:p.Arg259=
NM_001281474.2:c.675+7362A=	NP_001268403.1:n.675+7362A=
NR_104019.2:n.1106A=