Canonical Allele Identifier: CA2050152557

Gene: METTL25

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.82358894_82358895delinsCT , CM000674.2:g.82358894_82358895delinsCT	GRCh38
NC_000012.11:g.82752673_82752674delinsCT , CM000674.1:g.82752673_82752674delinsCT	GRCh37
NC_000012.10:g.81276804_81276805delinsCT	NCBI36
NG_053173.1:g.5489_5490delinsCT
NG_053173.2:g.5489_5490delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248306.8:c.259+70_259+71delinsCT MANE Select	ENSP00000248306.3:n.259+70_259+71delinsCT
ENST00000248306.7:c.259+70_259+71delinsCT	ENSP00000248306.3:n.259+70_259+71delinsCT
ENST00000547357.5:n.296+70_296+71delinsCT
ENST00000547985.1:n.366_367delinsCT
ENST00000548200.5:c.259+70_259+71delinsCT	ENSP00000446878.1:n.259+70_259+71delinsCT
ENST00000548569.5:n.297+70_297+71delinsCT
ENST00000550058.1:c.1_2delinsCT
NM_032230.2:c.259+70_259+71delinsCT	NP_115606.2:n.259+70_259+71delinsCT
XM_005269184.2:c.259+70_259+71delinsCT	XP_005269241.1:n.259+70_259+71delinsCT
XM_005269186.3:c.259+70_259+71delinsCT	XP_005269243.2:n.259+70_259+71delinsCT
XM_006719636.2:c.-25_-24delinsCT	XP_006719699.1:n.-25_-24delinsCT
XM_006719637.2:c.259+70_259+71delinsCT	XP_006719700.1:n.259+70_259+71delinsCT
XM_011538827.1:c.259+70_259+71delinsCT	XP_011537129.1:n.259+70_259+71delinsCT
XM_011538828.1:c.259+70_259+71delinsCT	XP_011537130.1:n.259+70_259+71delinsCT
XM_011538829.1:c.259+70_259+71delinsCT	XP_011537131.1:n.259+70_259+71delinsCT
XM_011538830.1:c.259+70_259+71delinsCT	XP_011537132.1:n.259+70_259+71delinsCT
XR_944768.1:n.419+70_419+71delinsCT
XR_944769.1:n.419+70_419+71delinsCT
NM_001319675.1:c.-25_-24delinsCT	NP_001306604.1:n.-25_-24delinsCT
NM_001347934.1:c.-72+70_-72+71delinsCT	NP_001334863.1:n.-72+70_-72+71delinsCT
NR_144940.1:n.328+70_328+71delinsCT
NR_144941.1:n.328+70_328+71delinsCT
NR_144942.1:n.398_399delinsCT
NR_144943.1:n.398_399delinsCT
XM_005269186.5:c.259+70_259+71delinsCT	XP_005269243.2:n.259+70_259+71delinsCT
XM_011538827.3:c.259+70_259+71delinsCT	XP_011537129.1:n.259+70_259+71delinsCT
XM_011538828.3:c.259+70_259+71delinsCT	XP_011537130.1:n.259+70_259+71delinsCT
XM_011538829.3:c.259+70_259+71delinsCT	XP_011537131.1:n.259+70_259+71delinsCT
XM_017020021.1:c.-1206+70_-1206+71delinsCT	XP_016875510.1:n.-1206+70_-1206+71delinsCT
XR_001748891.2:n.325+70_325+71delinsCT
XR_001748893.2:n.325+70_325+71delinsCT
XR_001748894.2:n.325+70_325+71delinsCT
XR_001748895.2:n.325+70_325+71delinsCT
XR_001748897.2:n.325+70_325+71delinsCT
XR_001748898.2:n.325+70_325+71delinsCT
XR_944768.3:n.325+70_325+71delinsCT
NM_032230.3:c.259+70_259+71delinsCT MANE Select	NP_115606.2:n.259+70_259+71delinsCT
NM_001319675.2:c.-25_-24delinsCT	NP_001306604.1:n.-25_-24delinsCT
NM_001347934.2:c.-72+70_-72+71delinsCT	NP_001334863.1:n.-72+70_-72+71delinsCT
NR_144940.2:n.296+70_296+71delinsCT
NR_144941.2:n.296+70_296+71delinsCT
NR_144942.2:n.366_367delinsCT
NR_144943.2:n.366_367delinsCT