Canonical Allele Identifier: CA516925804

Gene: MSN

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.65729578C>G , CM000685.2:g.65729578C>G	GRCh38
NC_000023.10:g.64949440C>G , CM000685.1:g.64949440C>G	GRCh37
NC_000023.9:g.64866165C>G	NCBI36
NG_012516.1:g.66930C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697133.1:c.300C>G	ENSP00000513131.1:p.Leu100=
ENST00000697134.1:c.*305C>G	ENSP00000513132.1:n.*305C>G
ENST00000697135.1:n.521C>G
ENST00000697137.1:c.300C>G	ENSP00000513133.1:p.Leu100=
ENST00000697138.1:c.300C>G	ENSP00000513134.1:p.Leu100=
ENST00000697140.1:n.447C>G
ENST00000697141.1:n.710C>G
ENST00000360270.7:c.333C>G MANE Select	ENSP00000353408.5:p.Leu111=
ENST00000360270.6:c.333C>G	ENSP00000353408.5:p.Leu111=
ENST00000609672.5:c.300C>G	ENSP00000477441.1:p.Leu100=
NM_002444.2:c.333C>G	NP_002435.1:p.Leu111=
XM_005262269.2:c.336C>G	XP_005262326.1:p.Leu112=
XM_011530959.1:c.432C>G	XP_011529261.1:p.Leu144=
XM_011530960.1:c.300C>G	XP_011529262.1:p.Leu100=
XM_017029545.1:c.300C>G	XP_016885034.1:p.Leu100=
XM_017029546.1:c.300C>G	XP_016885035.1:p.Leu100=
NM_002444.3:c.333C>G MANE Select	NP_002435.1:p.Leu111=