Canonical Allele Identifier: CA516929117

Gene: MSN

Linked Data

• MyVariant Identifiers: chrX:g.64959689C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.65739827C>T , CM000685.2:g.65739827C>T	GRCh38
NC_000023.10:g.64959689C>T , CM000685.1:g.64959689C>T	GRCh37
NC_000023.9:g.64876414C>T	NCBI36
NG_012516.1:g.77179C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000697133.1:c.1635C>T	ENSP00000513131.1:p.Tyr545=
ENST00000697134.1:c.*1640C>T	ENSP00000513132.1:n.*1640C>T
ENST00000697135.1:n.3250C>T
ENST00000697137.1:c.1635C>T	ENSP00000513133.1:p.Tyr545=
ENST00000697138.1:c.1635C>T	ENSP00000513134.1:p.Tyr545=
ENST00000697140.1:n.1782C>T
ENST00000697142.1:n.1585C>T
ENST00000360270.7:c.1668C>T MANE Select	ENSP00000353408.5:p.Tyr556=
ENST00000360270.6:c.1668C>T	ENSP00000353408.5:p.Tyr556=
NM_002444.2:c.1668C>T	NP_002435.1:p.Tyr556=
XM_005262269.2:c.1671C>T	XP_005262326.1:p.Tyr557=
XM_011530959.1:c.1767C>T	XP_011529261.1:p.Tyr589=
XM_011530960.1:c.1635C>T	XP_011529262.1:p.Tyr545=
XM_017029545.1:c.1635C>T	XP_016885034.1:p.Tyr545=
XM_017029546.1:c.1635C>T	XP_016885035.1:p.Tyr545=
NM_002444.3:c.1668C>T MANE Select	NP_002435.1:p.Tyr556=