Canonical Allele Identifier: CA1337695057

Gene: MLPH

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237527277T= , CM000664.2:g.237527277T=	GRCh38
NC_000002.11:g.238435920T= , CM000664.1:g.238435920T=	GRCh37
NC_000002.10:g.238100659T=	NCBI36
NG_007286.1:g.44991T= , LRG_83:g.44991T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264605.8:c.881-100T= MANE Select	ENSP00000264605.3:n.881-100T=
ENST00000264605.7:c.881-100T=	ENSP00000264605.3:n.881-100T=
ENST00000338530.8:c.881-100T=	ENSP00000341845.4:n.881-100T=
ENST00000409373.5:c.761-100T=	ENSP00000386780.1:n.761-100T=
ENST00000410032.5:c.675+7248T=	ENSP00000386338.1:n.675+7248T=
ENST00000436965.5:c.79-52T=
ENST00000437893.5:c.300+1472T=	ENSP00000412438.1:n.300+1472T=
ENST00000464123.5:n.946-100T=
ENST00000468178.5:n.1092-100T=
ENST00000478712.5:n.560-100T=
ENST00000482528.1:n.133-100T=
ENST00000485956.1:n.257-100T=
ENST00000494110.5:n.561-100T=
ENST00000495439.5:n.1258-100T=
NM_001042467.2:c.881-100T=	NP_001035932.1:n.881-100T=
NM_001281473.1:c.761-100T=	NP_001268402.1:n.761-100T=
NM_001281474.1:c.675+7248T=	NP_001268403.1:n.675+7248T=
NM_024101.6:c.881-100T=	NP_077006.1:n.881-100T=
NR_104019.1:n.1124-100T=
XM_006712737.1:c.761-100T=	XP_006712800.1:n.761-100T=
XM_006712739.1:c.881-100T=	XP_006712802.1:n.881-100T=
XM_006712740.1:c.761-100T=	XP_006712803.1:n.761-100T=
XM_011511811.1:c.881-100T=	XP_011510113.1:n.881-100T=
XM_011511812.1:c.446-100T=	XP_011510114.1:n.446-100T=
XR_923025.1:n.1092-100T=
XM_017004893.1:c.881-100T=	XP_016860382.1:n.881-100T=
XM_017004894.2:c.881-100T=	XP_016860383.1:n.881-100T=
NM_024101.7:c.881-100T= MANE Select	NP_077006.1:n.881-100T=
NM_001042467.3:c.881-100T=	NP_001035932.1:n.881-100T=
NM_001281473.2:c.761-100T=	NP_001268402.1:n.761-100T=
NM_001281474.2:c.675+7248T=	NP_001268403.1:n.675+7248T=
NR_104019.2:n.1092-100T=