Canonical Allele Identifier: CA413414784

Gene: MSN

Linked Data

• MyVariant Identifiers: chrX:g.64959682A>C (hg19) ; chrX:g.65739820A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.65739820A>C , CM000685.2:g.65739820A>C	GRCh38
NC_000023.10:g.64959682A>C , CM000685.1:g.64959682A>C	GRCh37
NC_000023.9:g.64876407A>C	NCBI36
NG_012516.1:g.77172A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000697133.1:c.1628A>C	ENSP00000513131.1:p.Asp543Ala
ENST00000697134.1:c.*1633A>C	ENSP00000513132.1:n.*1633A>C
ENST00000697135.1:n.3243A>C
ENST00000697137.1:c.1628A>C	ENSP00000513133.1:p.Asp543Ala
ENST00000697138.1:c.1628A>C	ENSP00000513134.1:p.Asp543Ala
ENST00000697140.1:n.1775A>C
ENST00000697142.1:n.1578A>C
ENST00000360270.7:c.1661A>C MANE Select	ENSP00000353408.5:p.Asp554Ala
ENST00000360270.6:c.1661A>C	ENSP00000353408.5:p.Asp554Ala
NM_002444.2:c.1661A>C	NP_002435.1:p.Asp554Ala
XM_005262269.2:c.1664A>C	XP_005262326.1:p.Asp555Ala
XM_011530959.1:c.1760A>C	XP_011529261.1:p.Asp587Ala
XM_011530960.1:c.1628A>C	XP_011529262.1:p.Asp543Ala
XM_017029545.1:c.1628A>C	XP_016885034.1:p.Asp543Ala
XM_017029546.1:c.1628A>C	XP_016885035.1:p.Asp543Ala
NM_002444.3:c.1661A>C MANE Select	NP_002435.1:p.Asp554Ala