Canonical Allele Identifier: CA516926248

Gene: MSN

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.65737182G>A , CM000685.2:g.65737182G>A	GRCh38
NC_000023.10:g.64957044G>A , CM000685.1:g.64957044G>A	GRCh37
NC_000023.9:g.64873769G>A	NCBI36
NG_012516.1:g.74534G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697133.1:c.1062G>A	ENSP00000513131.1:p.Leu354=
ENST00000697134.1:c.*1067G>A	ENSP00000513132.1:n.*1067G>A
ENST00000697135.1:n.2677G>A
ENST00000697137.1:c.1062G>A	ENSP00000513133.1:p.Leu354=
ENST00000697138.1:c.1062G>A	ENSP00000513134.1:p.Leu354=
ENST00000697140.1:n.1209G>A
ENST00000697142.1:n.1012G>A
ENST00000360270.7:c.1095G>A MANE Select	ENSP00000353408.5:p.Leu365=
ENST00000360270.6:c.1095G>A	ENSP00000353408.5:p.Leu365=
NM_002444.2:c.1095G>A	NP_002435.1:p.Leu365=
XM_005262269.2:c.1098G>A	XP_005262326.1:p.Leu366=
XM_011530959.1:c.1194G>A	XP_011529261.1:p.Leu398=
XM_011530960.1:c.1062G>A	XP_011529262.1:p.Leu354=
XM_017029545.1:c.1062G>A	XP_016885034.1:p.Leu354=
XM_017029546.1:c.1062G>A	XP_016885035.1:p.Leu354=
NM_002444.3:c.1095G>A MANE Select	NP_002435.1:p.Leu365=