Canonical Allele Identifier: CA10434617

Gene: MSN

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.65737193C>G , CM000685.2:g.65737193C>G	GRCh38
NC_000023.10:g.64957055C>G , CM000685.1:g.64957055C>G	GRCh37
NC_000023.9:g.64873780C>G	NCBI36
NG_012516.1:g.74545C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697133.1:c.1073C>G	ENSP00000513131.1:p.Thr358Ser
ENST00000697134.1:c.*1078C>G	ENSP00000513132.1:n.*1078C>G
ENST00000697135.1:n.2688C>G
ENST00000697137.1:c.1073C>G	ENSP00000513133.1:p.Thr358Ser
ENST00000697138.1:c.1073C>G	ENSP00000513134.1:p.Thr358Ser
ENST00000697140.1:n.1220C>G
ENST00000697142.1:n.1023C>G
ENST00000360270.7:c.1106C>G MANE Select	ENSP00000353408.5:p.Thr369Ser
ENST00000360270.6:c.1106C>G	ENSP00000353408.5:p.Thr369Ser
NM_002444.2:c.1106C>G	NP_002435.1:p.Thr369Ser
XM_005262269.2:c.1109C>G	XP_005262326.1:p.Thr370Ser
XM_011530959.1:c.1205C>G	XP_011529261.1:p.Thr402Ser
XM_011530960.1:c.1073C>G	XP_011529262.1:p.Thr358Ser
XM_017029545.1:c.1073C>G	XP_016885034.1:p.Thr358Ser
XM_017029546.1:c.1073C>G	XP_016885035.1:p.Thr358Ser
NM_002444.3:c.1106C>G MANE Select	NP_002435.1:p.Thr369Ser