Canonical Allele Identifier: CA10434512

Gene: MSN

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.65731093C>T , CM000685.2:g.65731093C>T	GRCh38
NC_000023.10:g.64950955C>T , CM000685.1:g.64950955C>T	GRCh37
NC_000023.9:g.64867680C>T	NCBI36
NG_012516.1:g.68445C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_002444.3:c.468-14C>T MANE Select	NP_002435.1:n.468-14C>T
ENST00000360270.7:c.468-14C>T MANE Select	ENSP00000353408.5:n.468-14C>T
NM_002444.2:c.468-14C>T	NP_002435.1:n.468-14C>T
ENST00000360270.6:c.468-14C>T	ENSP00000353408.5:n.468-14C>T
ENST00000697133.1:c.435-14C>T	ENSP00000513131.1:n.435-14C>T
ENST00000697134.1:c.*440-14C>T	ENSP00000513132.1:n.*440-14C>T
ENST00000697135.1:n.2036C>T
ENST00000697137.1:c.435-14C>T	ENSP00000513133.1:n.435-14C>T
ENST00000697138.1:c.435-14C>T	ENSP00000513134.1:n.435-14C>T
ENST00000697140.1:n.582-14C>T
XM_005262269.2:c.471-14C>T	XP_005262326.1:n.471-14C>T
XM_011530959.1:c.567-14C>T	XP_011529261.1:n.567-14C>T
XM_011530960.1:c.435-14C>T	XP_011529262.1:n.435-14C>T
XM_017029545.1:c.435-14C>T	XP_016885034.1:n.435-14C>T
XM_017029546.1:c.435-14C>T	XP_016885035.1:n.435-14C>T