Canonical Allele Identifier: CA385896117

Gene: METTL25

Linked Data

• MyVariant Identifiers: chr12:g.82752594T>C (hg19) ; chr12:g.82358815T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.82358815T>C , CM000674.2:g.82358815T>C	GRCh38
NC_000012.11:g.82752594T>C , CM000674.1:g.82752594T>C	GRCh37
NC_000012.10:g.81276725T>C	NCBI36
NG_053173.1:g.5410T>C
NG_053173.2:g.5410T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248306.8:c.250T>C MANE Select	ENSP00000248306.3:p.Trp84Arg
ENST00000248306.7:c.250T>C	ENSP00000248306.3:p.Trp84Arg
ENST00000547357.5:n.287T>C
ENST00000547985.1:n.287T>C
ENST00000548200.5:c.250T>C	ENSP00000446878.1:p.Trp84Arg
ENST00000548569.5:n.288T>C
NM_032230.2:c.250T>C	NP_115606.2:p.Trp84Arg
XM_005269184.2:c.250T>C	XP_005269241.1:p.Trp84Arg
XM_005269186.3:c.250T>C	XP_005269243.2:p.Trp84Arg
XM_006719636.2:c.-104T>C	XP_006719699.1:n.-104T>C
XM_006719637.2:c.250T>C	XP_006719700.1:p.Trp84Arg
XM_011538827.1:c.250T>C	XP_011537129.1:p.Trp84Arg
XM_011538828.1:c.250T>C	XP_011537130.1:p.Trp84Arg
XM_011538829.1:c.250T>C	XP_011537131.1:p.Trp84Arg
XM_011538830.1:c.250T>C	XP_011537132.1:p.Trp84Arg
XR_944768.1:n.410T>C
XR_944769.1:n.410T>C
NM_001319675.1:c.-104T>C	NP_001306604.1:n.-104T>C
NM_001347934.1:c.-81T>C	NP_001334863.1:n.-81T>C
NR_144940.1:n.319T>C
NR_144941.1:n.319T>C
NR_144942.1:n.319T>C
NR_144943.1:n.319T>C
XM_005269186.5:c.250T>C	XP_005269243.2:p.Trp84Arg
XM_011538827.3:c.250T>C	XP_011537129.1:p.Trp84Arg
XM_011538828.3:c.250T>C	XP_011537130.1:p.Trp84Arg
XM_011538829.3:c.250T>C	XP_011537131.1:p.Trp84Arg
XM_017020021.1:c.-1215T>C	XP_016875510.1:n.-1215T>C
XR_001748891.2:n.316T>C
XR_001748893.2:n.316T>C
XR_001748894.2:n.316T>C
XR_001748895.2:n.316T>C
XR_001748897.2:n.316T>C
XR_001748898.2:n.316T>C
XR_944768.3:n.316T>C
NM_032230.3:c.250T>C MANE Select	NP_115606.2:p.Trp84Arg
NM_001319675.2:c.-104T>C	NP_001306604.1:n.-104T>C
NM_001347934.2:c.-81T>C	NP_001334863.1:n.-81T>C
NR_144940.2:n.287T>C
NR_144941.2:n.287T>C
NR_144942.2:n.287T>C
NR_144943.2:n.287T>C