Canonical Allele Identifier: CA412066047

Gene: MSL3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.11765598C>G , CM000685.2:g.11765598C>G	GRCh38
NC_000023.10:g.11783717C>G , CM000685.1:g.11783717C>G	GRCh37
NC_000023.9:g.11693638C>G	NCBI36
NG_012564.1:g.12440C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312196.10:c.1040C>G MANE Select	ENSP00000312244.4:p.Ser347Cys
ENST00000337339.7:c.1040C>G	ENSP00000338078.2:p.Ser347Cys
ENST00000380691.3:c.346C>G	ENSP00000370067.2:p.Leu116Val
ENST00000380693.8:c.539C>G	ENSP00000370069.4:p.Ser180Cys
ENST00000398527.7:c.1004C>G	ENSP00000381538.2:p.Ser335Cys
ENST00000467141.2:c.61C>G
ENST00000473380.2:n.2857C>G
ENST00000482871.6:c.542C>G	ENSP00000498064.1:p.Ser181Cys
ENST00000647599.1:c.61C>G
ENST00000647701.1:n.2582C>G
ENST00000647839.1:c.61C>G
ENST00000647857.1:c.1040C>G	ENSP00000497753.1:p.Ser347Cys
ENST00000647869.1:c.1037C>G	ENSP00000497615.1:p.Ser346Cys
ENST00000647985.1:n.3323C>G
ENST00000648013.1:c.542C>G	ENSP00000497518.1:p.Ser181Cys
ENST00000648207.1:n.2614C>G
ENST00000648287.1:c.61C>G
ENST00000648545.1:c.61C>G
ENST00000648614.1:c.*336C>G	ENSP00000497799.1:n.*336C>G
ENST00000648656.1:c.61C>G
ENST00000648692.1:c.61C>G
ENST00000648889.1:n.2163C>G
ENST00000648918.1:n.3683C>G
ENST00000649078.1:c.542C>G	ENSP00000498017.1:p.Ser181Cys
ENST00000649130.1:c.940C>G
ENST00000649271.1:c.542C>G	ENSP00000496967.1:p.Ser181Cys
ENST00000649308.1:n.1108C>G
ENST00000649420.1:c.1C>G
ENST00000649602.1:c.542C>G	ENSP00000498168.1:p.Ser181Cys
ENST00000649649.1:c.593C>G	ENSP00000497137.1:p.Ser198Cys
ENST00000649684.1:n.2625C>G
ENST00000649685.1:c.593C>G	ENSP00000497496.1:p.Ser198Cys
ENST00000649785.1:c.542C>G	ENSP00000496803.1:p.Ser181Cys
ENST00000649797.1:c.542C>G	ENSP00000498062.1:p.Ser181Cys
ENST00000649851.1:c.542C>G	ENSP00000497132.1:p.Ser181Cys
ENST00000649988.1:n.3715C>G
ENST00000650050.1:n.2103C>G
ENST00000650106.1:c.61C>G
ENST00000650215.1:c.593C>G	ENSP00000496944.1:p.Ser198Cys
ENST00000650370.1:c.*846C>G	ENSP00000498088.1:n.*846C>G
ENST00000650628.1:c.542C>G	ENSP00000496838.1:p.Ser181Cys
ENST00000312196.8:c.1040C>G	ENSP00000312244.4:p.Ser347Cys
ENST00000337339.6:c.1040C>G	ENSP00000338078.2:p.Ser347Cys
ENST00000361672.6:c.593C>G	ENSP00000354562.2:p.Ser198Cys
ENST00000380691.2:c.346C>G	ENSP00000370067.2:p.Leu116Val
ENST00000380692.6:c.542C>G	ENSP00000370068.2:p.Ser181Cys
ENST00000380693.7:c.542C>G	ENSP00000370069.3:p.Ser181Cys
ENST00000398527.6:c.1004C>G	ENSP00000381538.2:p.Ser335Cys
ENST00000468149.5:c.*573C>G	ENSP00000418673.1:n.*573C>G
NM_001193270.2:c.1004C>G	NP_001180199.1:p.Ser335Cys
NM_001282174.1:c.593C>G	NP_001269103.1:p.Ser198Cys
NM_006800.3:c.542C>G	NP_006791.2:p.Ser181Cys
NM_078628.1:c.1040C>G	NP_523352.1:p.Ser347Cys
NM_078629.3:c.1040C>G	NP_523353.2:p.Ser347Cys
XM_005274440.2:c.542C>G	XP_005274497.1:p.Ser181Cys
XM_006724461.1:c.593C>G	XP_006724524.1:p.Ser198Cys
XM_011545442.1:c.1040C>G	XP_011543744.1:p.Ser347Cys
XM_011545443.1:c.1040C>G	XP_011543745.1:p.Ser347Cys
XM_011545444.1:c.1040C>G	XP_011543746.1:p.Ser347Cys
XM_005274440.3:c.542C>G	XP_005274497.1:p.Ser181Cys
XM_011545442.3:c.1040C>G	XP_011543744.1:p.Ser347Cys
XR_001755649.2:n.1092C>G
NM_006800.4:c.542C>G	NP_006791.2:p.Ser181Cys
NM_078629.4:c.1040C>G MANE Select	NP_523353.2:p.Ser347Cys
NM_078628.2:c.1040C>G	NP_523352.1:p.Ser347Cys