Canonical Allele Identifier: CA2050152671

Gene: METTL25

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.82359060_82359061delinsGA , CM000674.2:g.82359060_82359061delinsGA	GRCh38
NC_000012.11:g.82752839_82752840delinsGA , CM000674.1:g.82752839_82752840delinsGA	GRCh37
NC_000012.10:g.81276970_81276971delinsGA	NCBI36
NG_053173.1:g.5655_5656delinsGA
NG_053173.2:g.5655_5656delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248306.8:c.259+236_259+237delinsGA MANE Select	ENSP00000248306.3:n.259+236_259+237delinsGA
ENST00000248306.7:c.259+236_259+237delinsGA	ENSP00000248306.3:n.259+236_259+237delinsGA
ENST00000547357.5:n.296+236_296+237delinsGA
ENST00000547985.1:n.388+144_388+145delinsGA
ENST00000548200.5:c.259+236_259+237delinsGA	ENSP00000446878.1:n.259+236_259+237delinsGA
ENST00000548569.5:n.297+236_297+237delinsGA
ENST00000550058.1:c.23+144_23+145delinsGA
NM_032230.2:c.259+236_259+237delinsGA	NP_115606.2:n.259+236_259+237delinsGA
XM_005269184.2:c.259+236_259+237delinsGA	XP_005269241.1:n.259+236_259+237delinsGA
XM_005269186.3:c.259+236_259+237delinsGA	XP_005269243.2:n.259+236_259+237delinsGA
XM_006719636.2:c.-3+144_-3+145delinsGA	XP_006719699.1:n.-3+144_-3+145delinsGA
XM_006719637.2:c.259+236_259+237delinsGA	XP_006719700.1:n.259+236_259+237delinsGA
XM_011538827.1:c.259+236_259+237delinsGA	XP_011537129.1:n.259+236_259+237delinsGA
XM_011538828.1:c.259+236_259+237delinsGA	XP_011537130.1:n.259+236_259+237delinsGA
XM_011538829.1:c.259+236_259+237delinsGA	XP_011537131.1:n.259+236_259+237delinsGA
XM_011538830.1:c.259+236_259+237delinsGA	XP_011537132.1:n.259+236_259+237delinsGA
XR_944768.1:n.419+236_419+237delinsGA
XR_944769.1:n.419+236_419+237delinsGA
NM_001319675.1:c.-3+144_-3+145delinsGA	NP_001306604.1:n.-3+144_-3+145delinsGA
NM_001347934.1:c.-72+236_-72+237delinsGA	NP_001334863.1:n.-72+236_-72+237delinsGA
NR_144940.1:n.328+236_328+237delinsGA
NR_144941.1:n.328+236_328+237delinsGA
NR_144942.1:n.420+144_420+145delinsGA
NR_144943.1:n.420+144_420+145delinsGA
XM_005269186.5:c.259+236_259+237delinsGA	XP_005269243.2:n.259+236_259+237delinsGA
XM_011538827.3:c.259+236_259+237delinsGA	XP_011537129.1:n.259+236_259+237delinsGA
XM_011538828.3:c.259+236_259+237delinsGA	XP_011537130.1:n.259+236_259+237delinsGA
XM_011538829.3:c.259+236_259+237delinsGA	XP_011537131.1:n.259+236_259+237delinsGA
XM_017020021.1:c.-1206+236_-1206+237delinsGA	XP_016875510.1:n.-1206+236_-1206+237delinsGA
XR_001748891.2:n.325+236_325+237delinsGA
XR_001748893.2:n.325+236_325+237delinsGA
XR_001748894.2:n.325+236_325+237delinsGA
XR_001748895.2:n.325+236_325+237delinsGA
XR_001748897.2:n.325+236_325+237delinsGA
XR_001748898.2:n.325+236_325+237delinsGA
XR_944768.3:n.325+236_325+237delinsGA
NM_032230.3:c.259+236_259+237delinsGA MANE Select	NP_115606.2:n.259+236_259+237delinsGA
NM_001319675.2:c.-3+144_-3+145delinsGA	NP_001306604.1:n.-3+144_-3+145delinsGA
NM_001347934.2:c.-72+236_-72+237delinsGA	NP_001334863.1:n.-72+236_-72+237delinsGA
NR_144940.2:n.296+236_296+237delinsGA
NR_144941.2:n.296+236_296+237delinsGA
NR_144942.2:n.388+144_388+145delinsGA
NR_144943.2:n.388+144_388+145delinsGA