Canonical Allele Identifier: CA10434515

Gene: MSN

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.65731167T>C , CM000685.2:g.65731167T>C	GRCh38
NC_000023.10:g.64951029T>C , CM000685.1:g.64951029T>C	GRCh37
NC_000023.9:g.64867754T>C	NCBI36
NG_012516.1:g.68519T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697133.1:c.495T>C	ENSP00000513131.1:p.His165=
ENST00000697134.1:c.*500T>C	ENSP00000513132.1:n.*500T>C
ENST00000697135.1:n.2110T>C
ENST00000697137.1:c.495T>C	ENSP00000513133.1:p.His165=
ENST00000697138.1:c.495T>C	ENSP00000513134.1:p.His165=
ENST00000697140.1:n.642T>C
ENST00000360270.7:c.528T>C MANE Select	ENSP00000353408.5:p.His176=
ENST00000360270.6:c.528T>C	ENSP00000353408.5:p.His176=
NM_002444.2:c.528T>C	NP_002435.1:p.His176=
XM_005262269.2:c.531T>C	XP_005262326.1:p.His177=
XM_011530959.1:c.627T>C	XP_011529261.1:p.His209=
XM_011530960.1:c.495T>C	XP_011529262.1:p.His165=
XM_017029545.1:c.495T>C	XP_016885034.1:p.His165=
XM_017029546.1:c.495T>C	XP_016885035.1:p.His165=
NM_002444.3:c.528T>C MANE Select	NP_002435.1:p.His176=