Canonical Allele Identifier: CA692507519

Gene: METTL25

Linked Data

• dbSNP Id: rs1186843150
• gnomAD v4: 12-82359014-CTCTT-C
• MyVariant Identifiers: chr12:g.82752794_82752797del (hg19) ; chr12:g.82359015_82359018del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.82359020_82359023del , CM000674.2:g.82359020_82359023del	GRCh38
NC_000012.11:g.82752799_82752802del , CM000674.1:g.82752799_82752802del	GRCh37
NC_000012.10:g.81276930_81276933del	NCBI36
NG_053173.1:g.5615_5618del
NG_053173.2:g.5615_5618del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248306.8:c.259+196_259+199del MANE Select	ENSP00000248306.3:n.259+196_259+199del
ENST00000248306.7:c.259+196_259+199del	ENSP00000248306.3:n.259+196_259+199del
ENST00000547357.5:n.296+196_296+199del
ENST00000547985.1:n.388+104_388+107del
ENST00000548200.5:c.259+196_259+199del	ENSP00000446878.1:n.259+196_259+199del
ENST00000548569.5:n.297+196_297+199del
ENST00000550058.1:c.23+104_23+107del
NM_032230.2:c.259+196_259+199del	NP_115606.2:n.259+196_259+199del
XM_005269184.2:c.259+196_259+199del	XP_005269241.1:n.259+196_259+199del
XM_005269186.3:c.259+196_259+199del	XP_005269243.2:n.259+196_259+199del
XM_006719636.2:c.-3+104_-3+107del	XP_006719699.1:n.-3+104_-3+107del
XM_006719637.2:c.259+196_259+199del	XP_006719700.1:n.259+196_259+199del
XM_011538827.1:c.259+196_259+199del	XP_011537129.1:n.259+196_259+199del
XM_011538828.1:c.259+196_259+199del	XP_011537130.1:n.259+196_259+199del
XM_011538829.1:c.259+196_259+199del	XP_011537131.1:n.259+196_259+199del
XM_011538830.1:c.259+196_259+199del	XP_011537132.1:n.259+196_259+199del
XR_944768.1:n.419+196_419+199del
XR_944769.1:n.419+196_419+199del
NM_001319675.1:c.-3+104_-3+107del	NP_001306604.1:n.-3+104_-3+107del
NM_001347934.1:c.-72+196_-72+199del	NP_001334863.1:n.-72+196_-72+199del
NR_144940.1:n.328+196_328+199del
NR_144941.1:n.328+196_328+199del
NR_144942.1:n.420+104_420+107del
NR_144943.1:n.420+104_420+107del
XM_005269186.5:c.259+196_259+199del	XP_005269243.2:n.259+196_259+199del
XM_011538827.3:c.259+196_259+199del	XP_011537129.1:n.259+196_259+199del
XM_011538828.3:c.259+196_259+199del	XP_011537130.1:n.259+196_259+199del
XM_011538829.3:c.259+196_259+199del	XP_011537131.1:n.259+196_259+199del
XM_017020021.1:c.-1206+196_-1206+199del	XP_016875510.1:n.-1206+196_-1206+199del
XR_001748891.2:n.325+196_325+199del
XR_001748893.2:n.325+196_325+199del
XR_001748894.2:n.325+196_325+199del
XR_001748895.2:n.325+196_325+199del
XR_001748897.2:n.325+196_325+199del
XR_001748898.2:n.325+196_325+199del
XR_944768.3:n.325+196_325+199del
NM_032230.3:c.259+196_259+199del MANE Select	NP_115606.2:n.259+196_259+199del
NM_001319675.2:c.-3+104_-3+107del	NP_001306604.1:n.-3+104_-3+107del
NM_001347934.2:c.-72+196_-72+199del	NP_001334863.1:n.-72+196_-72+199del
NR_144940.2:n.296+196_296+199del
NR_144941.2:n.296+196_296+199del
NR_144942.2:n.388+104_388+107del
NR_144943.2:n.388+104_388+107del