Canonical Allele Identifier: CA109758565
Community Standard Title: NM_006745.5(MSMO1):c.405-161C>T
Gene: MSMO1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.165338491C>T , CM000666.2:g.165338491C>T GRCh38
NC_000004.11:g.166259643C>T , CM000666.1:g.166259643C>T GRCh37
NC_000004.10:g.166479093C>T NCBI36
NG_042288.1:g.15826C>T

Transcript Alleles

HGVS Amino-acid Change
NM_006745.5:c.405-161C>T MANE Select NP_006736.1:n.405-161C>T
ENST00000261507.11:c.405-161C>T MANE Select ENSP00000261507.6:n.405-161C>T
NM_001017369.2:c.12-161C>T NP_001017369.1:n.12-161C>T
NM_001017369.3:c.12-161C>T NP_001017369.1:n.12-161C>T
NM_006745.4:c.405-161C>T NP_006736.1:n.405-161C>T
ENST00000261507.10:c.405-161C>T ENSP00000261507.6:n.405-161C>T
ENST00000393766.6:c.12-161C>T ENSP00000377361.2:n.12-161C>T
ENST00000504317.1:c.405-161C>T ENSP00000423633.1:n.405-161C>T
ENST00000507013.5:c.405-161C>T ENSP00000425241.1:n.405-161C>T
XM_005263176.1:c.405-161C>T XP_005263233.1:n.405-161C>T
XM_005263176.2:c.405-161C>T XP_005263233.1:n.405-161C>T