Canonical Allele Identifier: CA1510035236

Gene: MSMO1

Genomic Alleles

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

Transcript Alleles

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