Canonical Allele Identifier: CA413413276

Gene: MSN

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.65737192A>T , CM000685.2:g.65737192A>T	GRCh38
NC_000023.10:g.64957054A>T , CM000685.1:g.64957054A>T	GRCh37
NC_000023.9:g.64873779A>T	NCBI36
NG_012516.1:g.74544A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697133.1:c.1072A>T	ENSP00000513131.1:p.Thr358Ser
ENST00000697134.1:c.*1077A>T	ENSP00000513132.1:n.*1077A>T
ENST00000697135.1:n.2687A>T
ENST00000697137.1:c.1072A>T	ENSP00000513133.1:p.Thr358Ser
ENST00000697138.1:c.1072A>T	ENSP00000513134.1:p.Thr358Ser
ENST00000697140.1:n.1219A>T
ENST00000697142.1:n.1022A>T
ENST00000360270.7:c.1105A>T MANE Select	ENSP00000353408.5:p.Thr369Ser
ENST00000360270.6:c.1105A>T	ENSP00000353408.5:p.Thr369Ser
NM_002444.2:c.1105A>T	NP_002435.1:p.Thr369Ser
XM_005262269.2:c.1108A>T	XP_005262326.1:p.Thr370Ser
XM_011530959.1:c.1204A>T	XP_011529261.1:p.Thr402Ser
XM_011530960.1:c.1072A>T	XP_011529262.1:p.Thr358Ser
XM_017029545.1:c.1072A>T	XP_016885034.1:p.Thr358Ser
XM_017029546.1:c.1072A>T	XP_016885035.1:p.Thr358Ser
NM_002444.3:c.1105A>T MANE Select	NP_002435.1:p.Thr369Ser