Canonical Allele Identifier: CA10434566

Gene: MSN

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.65735273G>A , CM000685.2:g.65735273G>A	GRCh38
NC_000023.10:g.64955135G>A , CM000685.1:g.64955135G>A	GRCh37
NC_000023.9:g.64871860G>A	NCBI36
NG_012516.1:g.72625G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697133.1:c.769G>A	ENSP00000513131.1:p.Val257Ile
ENST00000697134.1:c.*774G>A	ENSP00000513132.1:n.*774G>A
ENST00000697135.1:n.2384G>A
ENST00000697137.1:c.769G>A	ENSP00000513133.1:p.Val257Ile
ENST00000697138.1:c.769G>A	ENSP00000513134.1:p.Val257Ile
ENST00000697140.1:n.916G>A
ENST00000360270.7:c.802G>A MANE Select	ENSP00000353408.5:p.Val268Ile
ENST00000360270.6:c.802G>A	ENSP00000353408.5:p.Val268Ile
NM_002444.2:c.802G>A	NP_002435.1:p.Val268Ile
XM_005262269.2:c.805G>A	XP_005262326.1:p.Val269Ile
XM_011530959.1:c.901G>A	XP_011529261.1:p.Val301Ile
XM_011530960.1:c.769G>A	XP_011529262.1:p.Val257Ile
XM_017029545.1:c.769G>A	XP_016885034.1:p.Val257Ile
XM_017029546.1:c.769G>A	XP_016885035.1:p.Val257Ile
NM_002444.3:c.802G>A MANE Select	NP_002435.1:p.Val268Ile