Canonical Allele Identifier: CA2580101271

Gene: MSN

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.65733294C>T , CM000685.2:g.65733294C>T	GRCh38
NC_000023.10:g.64953156C>T , CM000685.1:g.64953156C>T	GRCh37
NC_000023.9:g.64869881C>T	NCBI36
NG_012516.1:g.70646C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_002444.3:c.795+14C>T MANE Select	NP_002435.1:n.795+14C>T
ENST00000360270.7:c.795+14C>T MANE Select	ENSP00000353408.5:n.795+14C>T
NM_002444.2:c.795+14C>T	NP_002435.1:n.795+14C>T
ENST00000360270.6:c.795+14C>T	ENSP00000353408.5:n.795+14C>T
ENST00000697133.1:c.762+14C>T	ENSP00000513131.1:n.762+14C>T
ENST00000697134.1:c.*767+14C>T	ENSP00000513132.1:n.*767+14C>T
ENST00000697135.1:n.2377+14C>T
ENST00000697137.1:c.762+14C>T	ENSP00000513133.1:n.762+14C>T
ENST00000697138.1:c.762+14C>T	ENSP00000513134.1:n.762+14C>T
ENST00000697140.1:n.909+14C>T
XM_005262269.2:c.798+14C>T	XP_005262326.1:n.798+14C>T
XM_011530959.1:c.894+14C>T	XP_011529261.1:n.894+14C>T
XM_011530960.1:c.762+14C>T	XP_011529262.1:n.762+14C>T
XM_017029545.1:c.762+14C>T	XP_016885034.1:n.762+14C>T
XM_017029546.1:c.762+14C>T	XP_016885035.1:n.762+14C>T