Canonical Allele Identifier: CA10434493

Gene: MSN

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.65729674G>A , CM000685.2:g.65729674G>A	GRCh38
NC_000023.10:g.64949536G>A , CM000685.1:g.64949536G>A	GRCh37
NC_000023.9:g.64866261G>A	NCBI36
NG_012516.1:g.67026G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697133.1:c.396G>A	ENSP00000513131.1:p.Lys132=
ENST00000697134.1:c.*401G>A	ENSP00000513132.1:n.*401G>A
ENST00000697135.1:n.617G>A
ENST00000697137.1:c.396G>A	ENSP00000513133.1:p.Lys132=
ENST00000697138.1:c.396G>A	ENSP00000513134.1:p.Lys132=
ENST00000697140.1:n.543G>A
ENST00000360270.7:c.429G>A MANE Select	ENSP00000353408.5:p.Lys143=
ENST00000360270.6:c.429G>A	ENSP00000353408.5:p.Lys143=
NM_002444.2:c.429G>A	NP_002435.1:p.Lys143=
XM_005262269.2:c.432G>A	XP_005262326.1:p.Lys144=
XM_011530959.1:c.528G>A	XP_011529261.1:p.Lys176=
XM_011530960.1:c.396G>A	XP_011529262.1:p.Lys132=
XM_017029545.1:c.396G>A	XP_016885034.1:p.Lys132=
XM_017029546.1:c.396G>A	XP_016885035.1:p.Lys132=
NM_002444.3:c.429G>A MANE Select	NP_002435.1:p.Lys143=