Canonical Allele Identifier: CA1337695157

Gene: MLPH

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237527494G= , CM000664.2:g.237527494G=	GRCh38
NC_000002.11:g.238436137G= , CM000664.1:g.238436137G=	GRCh37
NC_000002.10:g.238100876G=	NCBI36
NG_007286.1:g.45208G= , LRG_83:g.45208G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264605.8:c.998G= MANE Select	ENSP00000264605.3:p.Gly333=
ENST00000264605.7:c.998G=	ENSP00000264605.3:p.Gly333=
ENST00000338530.8:c.998G=	ENSP00000341845.4:p.Gly333=
ENST00000409373.5:c.878G=	ENSP00000386780.1:p.Gly293=
ENST00000410032.5:c.675+7465G=	ENSP00000386338.1:n.675+7465G=
ENST00000415753.5:c.60G=
ENST00000436965.5:c.244G=
ENST00000437893.5:c.300+1689G=	ENSP00000412438.1:n.300+1689G=
ENST00000464123.5:n.1063G=
ENST00000468178.5:n.1209G=
ENST00000478712.5:n.677G=
ENST00000482528.1:n.250G=
ENST00000485956.1:n.374G=
ENST00000494110.5:n.678G=
ENST00000495439.5:n.1375G=
NM_001042467.2:c.998G=	NP_001035932.1:p.Gly333=
NM_001281473.1:c.878G=	NP_001268402.1:p.Gly293=
NM_001281474.1:c.675+7465G=	NP_001268403.1:n.675+7465G=
NM_024101.6:c.998G=	NP_077006.1:p.Gly333=
NR_104019.1:n.1241G=
XM_006712737.1:c.878G=	XP_006712800.1:p.Gly293=
XM_006712739.1:c.998G=	XP_006712802.1:p.Gly333=
XM_006712740.1:c.878G=	XP_006712803.1:p.Gly293=
XM_011511811.1:c.998G=	XP_011510113.1:p.Gly333=
XM_011511812.1:c.563G=	XP_011510114.1:p.Gly188=
XR_923025.1:n.1209G=
XM_017004893.1:c.998G=	XP_016860382.1:p.Gly333=
XM_017004894.2:c.998G=	XP_016860383.1:p.Gly333=
NM_024101.7:c.998G= MANE Select	NP_077006.1:p.Gly333=
NM_001042467.3:c.998G=	NP_001035932.1:p.Gly333=
NM_001281473.2:c.878G=	NP_001268402.1:p.Gly293=
NM_001281474.2:c.675+7465G=	NP_001268403.1:n.675+7465G=
NR_104019.2:n.1209G=