Canonical Allele Identifier: CA358683122

Gene: MSMO1

Linked Data

• MyVariant Identifiers: chr4:g.166254537A>C (hg19) ; chr4:g.165333385A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.165333385A>C , CM000666.2:g.165333385A>C	GRCh38
NC_000004.11:g.166254537A>C , CM000666.1:g.166254537A>C	GRCh37
NC_000004.10:g.166473987A>C	NCBI36
NG_042288.1:g.10720A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261507.11:c.15A>C MANE Select	ENSP00000261507.6:p.Glu5Asp
ENST00000261507.10:c.15A>C	ENSP00000261507.6:p.Glu5Asp
ENST00000393766.6:c.-138-4404A>C	ENSP00000377361.2:n.-138-4404A>C
ENST00000504317.1:c.15A>C	ENSP00000423633.1:p.Glu5Asp
ENST00000505270.1:c.15A>C	ENSP00000425112.1:p.Glu5Asp
ENST00000507013.5:c.15A>C	ENSP00000425241.1:p.Glu5Asp
NM_001017369.2:c.-138-4404A>C	NP_001017369.1:n.-138-4404A>C
NM_006745.4:c.15A>C	NP_006736.1:p.Glu5Asp
XM_005263176.1:c.15A>C	XP_005263233.1:p.Glu5Asp
XM_005263176.2:c.15A>C	XP_005263233.1:p.Glu5Asp
NM_006745.5:c.15A>C MANE Select	NP_006736.1:p.Glu5Asp
NM_001017369.3:c.-138-4404A>C	NP_001017369.1:n.-138-4404A>C