Canonical Allele Identifier: CA11818571
Gene: MSMO1 HGNC NCBI

Linked Data

dbSNP Id: rs17046216

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.165334552T>A , CM000666.2:g.165334552T>A GRCh38
NC_000004.11:g.166255704T>A , CM000666.1:g.166255704T>A GRCh37
NC_000004.10:g.166475154T>A NCBI36
NG_042288.1:g.11887T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261507.11:c.255+927T>A MANE Select ENSP00000261507.6:n.255+927T>A
ENST00000261507.10:c.255+927T>A ENSP00000261507.6:n.255+927T>A
ENST00000393766.6:c.-138-3237T>A ENSP00000377361.2:n.-138-3237T>A
ENST00000504317.1:c.255+927T>A ENSP00000423633.1:n.255+927T>A
ENST00000507013.5:c.255+927T>A ENSP00000425241.1:n.255+927T>A
NM_001017369.2:c.-138-3237T>A NP_001017369.1:n.-138-3237T>A
NM_006745.4:c.255+927T>A NP_006736.1:n.255+927T>A
XM_005263176.1:c.255+927T>A XP_005263233.1:n.255+927T>A
XM_005263176.2:c.255+927T>A XP_005263233.1:n.255+927T>A
NM_006745.5:c.255+927T>A MANE Select NP_006736.1:n.255+927T>A
NM_001017369.3:c.-138-3237T>A NP_001017369.1:n.-138-3237T>A