Canonical Allele Identifier: CA330544731

Gene: MSN

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.65736791C>T , CM000685.2:g.65736791C>T	GRCh38
NC_000023.10:g.64956653C>T , CM000685.1:g.64956653C>T	GRCh37
NC_000023.9:g.64873378C>T	NCBI36
NG_012516.1:g.74143C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_002444.3:c.960-4C>T MANE Select	NP_002435.1:n.960-4C>T
ENST00000360270.7:c.960-4C>T MANE Select	ENSP00000353408.5:n.960-4C>T
NM_002444.2:c.960-4C>T	NP_002435.1:n.960-4C>T
ENST00000360270.6:c.960-4C>T	ENSP00000353408.5:n.960-4C>T
ENST00000697133.1:c.927-4C>T	ENSP00000513131.1:n.927-4C>T
ENST00000697134.1:c.*932-4C>T	ENSP00000513132.1:n.*932-4C>T
ENST00000697135.1:n.2542-4C>T
ENST00000697137.1:c.927-4C>T	ENSP00000513133.1:n.927-4C>T
ENST00000697138.1:c.927-4C>T	ENSP00000513134.1:n.927-4C>T
ENST00000697140.1:n.1074-4C>T
ENST00000697142.1:n.873C>T
XM_005262269.2:c.963-4C>T	XP_005262326.1:n.963-4C>T
XM_011530959.1:c.1059-4C>T	XP_011529261.1:n.1059-4C>T
XM_011530960.1:c.927-4C>T	XP_011529262.1:n.927-4C>T
XM_017029545.1:c.927-4C>T	XP_016885034.1:n.927-4C>T
XM_017029546.1:c.927-4C>T	XP_016885035.1:n.927-4C>T