Canonical Allele Identifier: CA2050152673

Gene: METTL25

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.82359064_82359066delinsCAG , CM000674.2:g.82359064_82359066delinsCAG	GRCh38
NC_000012.11:g.82752843_82752845delinsCAG , CM000674.1:g.82752843_82752845delinsCAG	GRCh37
NC_000012.10:g.81276974_81276976delinsCAG	NCBI36
NG_053173.1:g.5659_5661delinsCAG
NG_053173.2:g.5659_5661delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248306.8:c.259+240_259+242delinsCAG MANE Select	ENSP00000248306.3:n.259+240_259+242delinsCAG
ENST00000248306.7:c.259+240_259+242delinsCAG	ENSP00000248306.3:n.259+240_259+242delinsCAG
ENST00000547357.5:n.296+240_296+242delinsCAG
ENST00000547985.1:n.388+148_388+150delinsCAG
ENST00000548200.5:c.259+240_259+242delinsCAG	ENSP00000446878.1:n.259+240_259+242delinsCAG
ENST00000548569.5:n.297+240_297+242delinsCAG
ENST00000550058.1:c.23+148_23+150delinsCAG
NM_032230.2:c.259+240_259+242delinsCAG	NP_115606.2:n.259+240_259+242delinsCAG
XM_005269184.2:c.259+240_259+242delinsCAG	XP_005269241.1:n.259+240_259+242delinsCAG
XM_005269186.3:c.259+240_259+242delinsCAG	XP_005269243.2:n.259+240_259+242delinsCAG
XM_006719636.2:c.-3+148_-3+150delinsCAG	XP_006719699.1:n.-3+148_-3+150delinsCAG
XM_006719637.2:c.259+240_259+242delinsCAG	XP_006719700.1:n.259+240_259+242delinsCAG
XM_011538827.1:c.259+240_259+242delinsCAG	XP_011537129.1:n.259+240_259+242delinsCAG
XM_011538828.1:c.259+240_259+242delinsCAG	XP_011537130.1:n.259+240_259+242delinsCAG
XM_011538829.1:c.259+240_259+242delinsCAG	XP_011537131.1:n.259+240_259+242delinsCAG
XM_011538830.1:c.259+240_259+242delinsCAG	XP_011537132.1:n.259+240_259+242delinsCAG
XR_944768.1:n.419+240_419+242delinsCAG
XR_944769.1:n.419+240_419+242delinsCAG
NM_001319675.1:c.-3+148_-3+150delinsCAG	NP_001306604.1:n.-3+148_-3+150delinsCAG
NM_001347934.1:c.-72+240_-72+242delinsCAG	NP_001334863.1:n.-72+240_-72+242delinsCAG
NR_144940.1:n.328+240_328+242delinsCAG
NR_144941.1:n.328+240_328+242delinsCAG
NR_144942.1:n.420+148_420+150delinsCAG
NR_144943.1:n.420+148_420+150delinsCAG
XM_005269186.5:c.259+240_259+242delinsCAG	XP_005269243.2:n.259+240_259+242delinsCAG
XM_011538827.3:c.259+240_259+242delinsCAG	XP_011537129.1:n.259+240_259+242delinsCAG
XM_011538828.3:c.259+240_259+242delinsCAG	XP_011537130.1:n.259+240_259+242delinsCAG
XM_011538829.3:c.259+240_259+242delinsCAG	XP_011537131.1:n.259+240_259+242delinsCAG
XM_017020021.1:c.-1206+240_-1206+242delinsCAG	XP_016875510.1:n.-1206+240_-1206+242delinsCAG
XR_001748891.2:n.325+240_325+242delinsCAG
XR_001748893.2:n.325+240_325+242delinsCAG
XR_001748894.2:n.325+240_325+242delinsCAG
XR_001748895.2:n.325+240_325+242delinsCAG
XR_001748897.2:n.325+240_325+242delinsCAG
XR_001748898.2:n.325+240_325+242delinsCAG
XR_944768.3:n.325+240_325+242delinsCAG
NM_032230.3:c.259+240_259+242delinsCAG MANE Select	NP_115606.2:n.259+240_259+242delinsCAG
NM_001319675.2:c.-3+148_-3+150delinsCAG	NP_001306604.1:n.-3+148_-3+150delinsCAG
NM_001347934.2:c.-72+240_-72+242delinsCAG	NP_001334863.1:n.-72+240_-72+242delinsCAG
NR_144940.2:n.296+240_296+242delinsCAG
NR_144941.2:n.296+240_296+242delinsCAG
NR_144942.2:n.388+148_388+150delinsCAG
NR_144943.2:n.388+148_388+150delinsCAG