Canonical Allele Identifier: CA413414061

Gene: MSN

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.65739064A>C , CM000685.2:g.65739064A>C	GRCh38
NC_000023.10:g.64958926A>C , CM000685.1:g.64958926A>C	GRCh37
NC_000023.9:g.64875651A>C	NCBI36
NG_012516.1:g.76416A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697133.1:c.1406A>C	ENSP00000513131.1:p.Gln469Pro
ENST00000697134.1:c.*1411A>C	ENSP00000513132.1:n.*1411A>C
ENST00000697135.1:n.3021A>C
ENST00000697137.1:c.1406A>C	ENSP00000513133.1:p.Gln469Pro
ENST00000697138.1:c.1406A>C	ENSP00000513134.1:p.Gln469Pro
ENST00000697140.1:n.1553A>C
ENST00000697142.1:n.1356A>C
ENST00000360270.7:c.1439A>C MANE Select	ENSP00000353408.5:p.Gln480Pro
ENST00000360270.6:c.1439A>C	ENSP00000353408.5:p.Gln480Pro
NM_002444.2:c.1439A>C	NP_002435.1:p.Gln480Pro
XM_005262269.2:c.1442A>C	XP_005262326.1:p.Gln481Pro
XM_011530959.1:c.1538A>C	XP_011529261.1:p.Gln513Pro
XM_011530960.1:c.1406A>C	XP_011529262.1:p.Gln469Pro
XM_017029545.1:c.1406A>C	XP_016885034.1:p.Gln469Pro
XM_017029546.1:c.1406A>C	XP_016885035.1:p.Gln469Pro
NM_002444.3:c.1439A>C MANE Select	NP_002435.1:p.Gln480Pro