Canonical Allele Identifier: CA10348904

Gene: MSL3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.11765706A>G , CM000685.2:g.11765706A>G	GRCh38
NC_000023.10:g.11783825A>G , CM000685.1:g.11783825A>G	GRCh37
NC_000023.9:g.11693746A>G	NCBI36
NG_012564.1:g.12548A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312196.10:c.1148A>G MANE Select	ENSP00000312244.4:p.Lys383Arg
ENST00000337339.7:c.1148A>G	ENSP00000338078.2:p.Lys383Arg
ENST00000380691.3:c.454A>G	ENSP00000370067.2:n.454A>G
ENST00000380693.8:c.647A>G	ENSP00000370069.4:p.Lys216Arg
ENST00000398527.7:c.1112A>G	ENSP00000381538.2:p.Lys371Arg
ENST00000467141.2:c.169A>G
ENST00000473380.2:n.2965A>G
ENST00000482871.6:c.650A>G	ENSP00000498064.1:p.Lys217Arg
ENST00000647599.1:c.169A>G
ENST00000647701.1:n.2690A>G
ENST00000647839.1:c.169A>G
ENST00000647857.1:c.1148A>G	ENSP00000497753.1:p.Lys383Arg
ENST00000647869.1:c.1145A>G	ENSP00000497615.1:p.Lys382Arg
ENST00000647985.1:n.3431A>G
ENST00000648013.1:c.650A>G	ENSP00000497518.1:p.Lys217Arg
ENST00000648207.1:n.2722A>G
ENST00000648287.1:c.169A>G
ENST00000648545.1:c.169A>G
ENST00000648614.1:c.*444A>G	ENSP00000497799.1:n.*444A>G
ENST00000648656.1:c.169A>G
ENST00000648692.1:c.169A>G
ENST00000648889.1:n.2271A>G
ENST00000648918.1:n.3791A>G
ENST00000649078.1:c.650A>G	ENSP00000498017.1:p.Lys217Arg
ENST00000649130.1:c.1048A>G
ENST00000649271.1:c.650A>G	ENSP00000496967.1:p.Lys217Arg
ENST00000649308.1:n.1216A>G
ENST00000649420.1:c.109A>G
ENST00000649602.1:c.650A>G	ENSP00000498168.1:p.Lys217Arg
ENST00000649649.1:c.701A>G	ENSP00000497137.1:p.Lys234Arg
ENST00000649684.1:n.2733A>G
ENST00000649685.1:c.701A>G	ENSP00000497496.1:p.Lys234Arg
ENST00000649785.1:c.650A>G	ENSP00000496803.1:p.Lys217Arg
ENST00000649797.1:c.650A>G	ENSP00000498062.1:p.Lys217Arg
ENST00000649851.1:c.650A>G	ENSP00000497132.1:p.Lys217Arg
ENST00000649988.1:n.3823A>G
ENST00000650050.1:n.2211A>G
ENST00000650106.1:c.169A>G
ENST00000650215.1:c.701A>G	ENSP00000496944.1:p.Lys234Arg
ENST00000650370.1:c.*954A>G	ENSP00000498088.1:n.*954A>G
ENST00000650628.1:c.650A>G	ENSP00000496838.1:p.Lys217Arg
ENST00000312196.8:c.1148A>G	ENSP00000312244.4:p.Lys383Arg
ENST00000337339.6:c.1148A>G	ENSP00000338078.2:p.Lys383Arg
ENST00000361672.6:c.701A>G	ENSP00000354562.2:p.Lys234Arg
ENST00000380691.2:c.454A>G	ENSP00000370067.2:n.454A>G
ENST00000380693.7:c.650A>G	ENSP00000370069.3:p.Lys217Arg
ENST00000398527.6:c.1112A>G	ENSP00000381538.2:p.Lys371Arg
ENST00000467141.1:n.46A>G
ENST00000468149.5:c.*681A>G	ENSP00000418673.1:n.*681A>G
NM_001193270.2:c.1112A>G	NP_001180199.1:p.Lys371Arg
NM_001282174.1:c.701A>G	NP_001269103.1:p.Lys234Arg
NM_006800.3:c.650A>G	NP_006791.2:p.Lys217Arg
NM_078628.1:c.1148A>G	NP_523352.1:p.Lys383Arg
NM_078629.3:c.1148A>G	NP_523353.2:p.Lys383Arg
XM_005274440.2:c.650A>G	XP_005274497.1:p.Lys217Arg
XM_006724461.1:c.701A>G	XP_006724524.1:p.Lys234Arg
XM_011545442.1:c.1148A>G	XP_011543744.1:p.Lys383Arg
XM_011545443.1:c.1148A>G	XP_011543745.1:p.Lys383Arg
XM_011545444.1:c.1148A>G	XP_011543746.1:p.Lys383Arg
XM_005274440.3:c.650A>G	XP_005274497.1:p.Lys217Arg
XM_011545442.3:c.1148A>G	XP_011543744.1:p.Lys383Arg
XR_001755649.2:n.1200A>G
NM_006800.4:c.650A>G	NP_006791.2:p.Lys217Arg
NM_078629.4:c.1148A>G MANE Select	NP_523353.2:p.Lys383Arg
NM_078628.2:c.1148A>G	NP_523352.1:p.Lys383Arg