Canonical Allele Identifier: CA516926109

Gene: MSN

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.65735317C>G , CM000685.2:g.65735317C>G	GRCh38
NC_000023.10:g.64955179C>G , CM000685.1:g.64955179C>G	GRCh37
NC_000023.9:g.64871904C>G	NCBI36
NG_012516.1:g.72669C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697133.1:c.813C>G	ENSP00000513131.1:p.Ala271=
ENST00000697134.1:c.*818C>G	ENSP00000513132.1:n.*818C>G
ENST00000697135.1:n.2428C>G
ENST00000697137.1:c.813C>G	ENSP00000513133.1:p.Ala271=
ENST00000697138.1:c.813C>G	ENSP00000513134.1:p.Ala271=
ENST00000697140.1:n.960C>G
ENST00000360270.7:c.846C>G MANE Select	ENSP00000353408.5:p.Ala282=
ENST00000360270.6:c.846C>G	ENSP00000353408.5:p.Ala282=
NM_002444.2:c.846C>G	NP_002435.1:p.Ala282=
XM_005262269.2:c.849C>G	XP_005262326.1:p.Ala283=
XM_011530959.1:c.945C>G	XP_011529261.1:p.Ala315=
XM_011530960.1:c.813C>G	XP_011529262.1:p.Ala271=
XM_017029545.1:c.813C>G	XP_016885034.1:p.Ala271=
XM_017029546.1:c.813C>G	XP_016885035.1:p.Ala271=
NM_002444.3:c.846C>G MANE Select	NP_002435.1:p.Ala282=