Canonical Allele Identifier: CA2050152646

Gene: METTL25

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.82359014_82359018delinsCTCTT , CM000674.2:g.82359014_82359018delinsCTCTT	GRCh38
NC_000012.11:g.82752793_82752797delinsCTCTT , CM000674.1:g.82752793_82752797delinsCTCTT	GRCh37
NC_000012.10:g.81276924_81276928delinsCTCTT	NCBI36
NG_053173.1:g.5609_5613delinsCTCTT
NG_053173.2:g.5609_5613delinsCTCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248306.8:c.259+190_259+194delinsCTCTT MANE Select	ENSP00000248306.3:n.259+190_259+194delinsCTCTT
ENST00000248306.7:c.259+190_259+194delinsCTCTT	ENSP00000248306.3:n.259+190_259+194delinsCTCTT
ENST00000547357.5:n.296+190_296+194delinsCTCTT
ENST00000547985.1:n.388+98_388+102delinsCTCTT
ENST00000548200.5:c.259+190_259+194delinsCTCTT	ENSP00000446878.1:n.259+190_259+194delinsCTCTT
ENST00000548569.5:n.297+190_297+194delinsCTCTT
ENST00000550058.1:c.23+98_23+102delinsCTCTT
NM_032230.2:c.259+190_259+194delinsCTCTT	NP_115606.2:n.259+190_259+194delinsCTCTT
XM_005269184.2:c.259+190_259+194delinsCTCTT	XP_005269241.1:n.259+190_259+194delinsCTCTT
XM_005269186.3:c.259+190_259+194delinsCTCTT	XP_005269243.2:n.259+190_259+194delinsCTCTT
XM_006719636.2:c.-3+98_-3+102delinsCTCTT	XP_006719699.1:n.-3+98_-3+102delinsCTCTT
XM_006719637.2:c.259+190_259+194delinsCTCTT	XP_006719700.1:n.259+190_259+194delinsCTCTT
XM_011538827.1:c.259+190_259+194delinsCTCTT	XP_011537129.1:n.259+190_259+194delinsCTCTT
XM_011538828.1:c.259+190_259+194delinsCTCTT	XP_011537130.1:n.259+190_259+194delinsCTCTT
XM_011538829.1:c.259+190_259+194delinsCTCTT	XP_011537131.1:n.259+190_259+194delinsCTCTT
XM_011538830.1:c.259+190_259+194delinsCTCTT	XP_011537132.1:n.259+190_259+194delinsCTCTT
XR_944768.1:n.419+190_419+194delinsCTCTT
XR_944769.1:n.419+190_419+194delinsCTCTT
NM_001319675.1:c.-3+98_-3+102delinsCTCTT	NP_001306604.1:n.-3+98_-3+102delinsCTCTT
NM_001347934.1:c.-72+190_-72+194delinsCTCTT	NP_001334863.1:n.-72+190_-72+194delinsCTCTT
NR_144940.1:n.328+190_328+194delinsCTCTT
NR_144941.1:n.328+190_328+194delinsCTCTT
NR_144942.1:n.420+98_420+102delinsCTCTT
NR_144943.1:n.420+98_420+102delinsCTCTT
XM_005269186.5:c.259+190_259+194delinsCTCTT	XP_005269243.2:n.259+190_259+194delinsCTCTT
XM_011538827.3:c.259+190_259+194delinsCTCTT	XP_011537129.1:n.259+190_259+194delinsCTCTT
XM_011538828.3:c.259+190_259+194delinsCTCTT	XP_011537130.1:n.259+190_259+194delinsCTCTT
XM_011538829.3:c.259+190_259+194delinsCTCTT	XP_011537131.1:n.259+190_259+194delinsCTCTT
XM_017020021.1:c.-1206+190_-1206+194delinsCTCTT	XP_016875510.1:n.-1206+190_-1206+194delinsCTCTT
XR_001748891.2:n.325+190_325+194delinsCTCTT
XR_001748893.2:n.325+190_325+194delinsCTCTT
XR_001748894.2:n.325+190_325+194delinsCTCTT
XR_001748895.2:n.325+190_325+194delinsCTCTT
XR_001748897.2:n.325+190_325+194delinsCTCTT
XR_001748898.2:n.325+190_325+194delinsCTCTT
XR_944768.3:n.325+190_325+194delinsCTCTT
NM_032230.3:c.259+190_259+194delinsCTCTT MANE Select	NP_115606.2:n.259+190_259+194delinsCTCTT
NM_001319675.2:c.-3+98_-3+102delinsCTCTT	NP_001306604.1:n.-3+98_-3+102delinsCTCTT
NM_001347934.2:c.-72+190_-72+194delinsCTCTT	NP_001334863.1:n.-72+190_-72+194delinsCTCTT
NR_144940.2:n.296+190_296+194delinsCTCTT
NR_144941.2:n.296+190_296+194delinsCTCTT
NR_144942.2:n.388+98_388+102delinsCTCTT
NR_144943.2:n.388+98_388+102delinsCTCTT