Canonical Allele Identifier: CA16042218
Gene: MSN HGNC NCBI

Linked Data

ClinVar Variation Id: 372154
dbSNP Id: rs1057519074
gnomAD v4: X-65731150-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.65731150C>T , CM000685.2:g.65731150C>T GRCh38
NC_000023.10:g.64951012C>T , CM000685.1:g.64951012C>T GRCh37
NC_000023.9:g.64867737C>T NCBI36
NG_012516.1:g.68502C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000697133.1:c.478C>T ENSP00000513131.1:p.Arg160Trp
ENST00000697134.1:c.*483C>T ENSP00000513132.1:n.*483C>T
ENST00000697135.1:n.2093C>T
ENST00000697137.1:c.478C>T ENSP00000513133.1:p.Arg160Trp
ENST00000697138.1:c.478C>T ENSP00000513134.1:p.Arg160Trp
ENST00000697140.1:n.625C>T
ENST00000360270.7:c.511C>T MANE Select ENSP00000353408.5:p.Arg171Trp
ENST00000360270.6:c.511C>T ENSP00000353408.5:p.Arg171Trp
NM_002444.2:c.511C>T NP_002435.1:p.Arg171Trp
XM_005262269.2:c.514C>T XP_005262326.1:p.Arg172Trp
XM_011530959.1:c.610C>T XP_011529261.1:p.Arg204Trp
XM_011530960.1:c.478C>T XP_011529262.1:p.Arg160Trp
XM_017029545.1:c.478C>T XP_016885034.1:p.Arg160Trp
XM_017029546.1:c.478C>T XP_016885035.1:p.Arg160Trp
NM_002444.3:c.511C>T MANE Select NP_002435.1:p.Arg171Trp