Canonical Allele Identifier: CA2050152494

Gene: METTL25

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.82358810C= , CM000674.2:g.82358810C=	GRCh38
NC_000012.11:g.82752589C= , CM000674.1:g.82752589C=	GRCh37
NC_000012.10:g.81276720C=	NCBI36
NG_053173.1:g.5405C=
NG_053173.2:g.5405C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248306.8:c.245C= MANE Select	ENSP00000248306.3:p.Ala82=
ENST00000248306.7:c.245C=	ENSP00000248306.3:p.Ala82=
ENST00000547357.5:n.282C=
ENST00000547985.1:n.282C=
ENST00000548200.5:c.245C=	ENSP00000446878.1:p.Ala82=
ENST00000548569.5:n.283C=
NM_032230.2:c.245C=	NP_115606.2:p.Ala82=
XM_005269184.2:c.245C=	XP_005269241.1:p.Ala82=
XM_005269186.3:c.245C=	XP_005269243.2:p.Ala82=
XM_006719636.2:c.-109C=	XP_006719699.1:n.-109C=
XM_006719637.2:c.245C=	XP_006719700.1:p.Ala82=
XM_011538827.1:c.245C=	XP_011537129.1:p.Ala82=
XM_011538828.1:c.245C=	XP_011537130.1:p.Ala82=
XM_011538829.1:c.245C=	XP_011537131.1:p.Ala82=
XM_011538830.1:c.245C=	XP_011537132.1:p.Ala82=
XR_944768.1:n.405C=
XR_944769.1:n.405C=
NM_001319675.1:c.-109C=	NP_001306604.1:n.-109C=
NM_001347934.1:c.-86C=	NP_001334863.1:n.-86C=
NR_144940.1:n.314C=
NR_144941.1:n.314C=
NR_144942.1:n.314C=
NR_144943.1:n.314C=
XM_005269186.5:c.245C=	XP_005269243.2:p.Ala82=
XM_011538827.3:c.245C=	XP_011537129.1:p.Ala82=
XM_011538828.3:c.245C=	XP_011537130.1:p.Ala82=
XM_011538829.3:c.245C=	XP_011537131.1:p.Ala82=
XM_017020021.1:c.-1220C=	XP_016875510.1:n.-1220C=
XR_001748891.2:n.311C=
XR_001748893.2:n.311C=
XR_001748894.2:n.311C=
XR_001748895.2:n.311C=
XR_001748897.2:n.311C=
XR_001748898.2:n.311C=
XR_944768.3:n.311C=
NM_032230.3:c.245C= MANE Select	NP_115606.2:p.Ala82=
NM_001319675.2:c.-109C=	NP_001306604.1:n.-109C=
NM_001347934.2:c.-86C=	NP_001334863.1:n.-86C=
NR_144940.2:n.282C=
NR_144941.2:n.282C=
NR_144942.2:n.282C=
NR_144943.2:n.282C=