Canonical Allele Identifier: CA2050152491

Gene: METTL25

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.82358804_82358816delinsTGGAAGCAGAGTG , CM000674.2:g.82358804_82358816delinsTGGAAGCAGAGTG	GRCh38
NC_000012.11:g.82752583_82752595delinsTGGAAGCAGAGTG , CM000674.1:g.82752583_82752595delinsTGGAAGCAGAGTG	GRCh37
NC_000012.10:g.81276714_81276726delinsTGGAAGCAGAGTG	NCBI36
NG_053173.1:g.5399_5411delinsTGGAAGCAGAGTG
NG_053173.2:g.5399_5411delinsTGGAAGCAGAGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248306.8:c.239_251delinsTGGAAGCAGAGTG MANE Select	ENSP00000248306.3:p.Val80=
ENST00000248306.7:c.239_251delinsTGGAAGCAGAGTG	ENSP00000248306.3:p.Val80=
ENST00000547357.5:n.276_288delinsTGGAAGCAGAGTG
ENST00000547985.1:n.276_288delinsTGGAAGCAGAGTG
ENST00000548200.5:c.239_251delinsTGGAAGCAGAGTG	ENSP00000446878.1:p.Val80=
ENST00000548569.5:n.277_289delinsTGGAAGCAGAGTG
NM_032230.2:c.239_251delinsTGGAAGCAGAGTG	NP_115606.2:p.Val80=
XM_005269184.2:c.239_251delinsTGGAAGCAGAGTG	XP_005269241.1:p.Val80=
XM_005269186.3:c.239_251delinsTGGAAGCAGAGTG	XP_005269243.2:p.Val80=
XM_006719636.2:c.-115_-103delinsTGGAAGCAGAGTG	XP_006719699.1:n.-115_-103delinsTGGAAGCAGAGTG
XM_006719637.2:c.239_251delinsTGGAAGCAGAGTG	XP_006719700.1:p.Val80=
XM_011538827.1:c.239_251delinsTGGAAGCAGAGTG	XP_011537129.1:p.Val80=
XM_011538828.1:c.239_251delinsTGGAAGCAGAGTG	XP_011537130.1:p.Val80=
XM_011538829.1:c.239_251delinsTGGAAGCAGAGTG	XP_011537131.1:p.Val80=
XM_011538830.1:c.239_251delinsTGGAAGCAGAGTG	XP_011537132.1:p.Val80=
XR_944768.1:n.399_411delinsTGGAAGCAGAGTG
XR_944769.1:n.399_411delinsTGGAAGCAGAGTG
NM_001319675.1:c.-115_-103delinsTGGAAGCAGAGTG	NP_001306604.1:n.-115_-103delinsTGGAAGCAGAGTG
NM_001347934.1:c.-92_-80delinsTGGAAGCAGAGTG	NP_001334863.1:n.-92_-80delinsTGGAAGCAGAGTG
NR_144940.1:n.308_320delinsTGGAAGCAGAGTG
NR_144941.1:n.308_320delinsTGGAAGCAGAGTG
NR_144942.1:n.308_320delinsTGGAAGCAGAGTG
NR_144943.1:n.308_320delinsTGGAAGCAGAGTG
XM_005269186.5:c.239_251delinsTGGAAGCAGAGTG	XP_005269243.2:p.Val80=
XM_011538827.3:c.239_251delinsTGGAAGCAGAGTG	XP_011537129.1:p.Val80=
XM_011538828.3:c.239_251delinsTGGAAGCAGAGTG	XP_011537130.1:p.Val80=
XM_011538829.3:c.239_251delinsTGGAAGCAGAGTG	XP_011537131.1:p.Val80=
XM_017020021.1:c.-1226_-1214delinsTGGAAGCAGAGTG	XP_016875510.1:n.-1226_-1214delinsTGGAAGCAGAGTG
XR_001748891.2:n.305_317delinsTGGAAGCAGAGTG
XR_001748893.2:n.305_317delinsTGGAAGCAGAGTG
XR_001748894.2:n.305_317delinsTGGAAGCAGAGTG
XR_001748895.2:n.305_317delinsTGGAAGCAGAGTG
XR_001748897.2:n.305_317delinsTGGAAGCAGAGTG
XR_001748898.2:n.305_317delinsTGGAAGCAGAGTG
XR_944768.3:n.305_317delinsTGGAAGCAGAGTG
NM_032230.3:c.239_251delinsTGGAAGCAGAGTG MANE Select	NP_115606.2:p.Val80=
NM_001319675.2:c.-115_-103delinsTGGAAGCAGAGTG	NP_001306604.1:n.-115_-103delinsTGGAAGCAGAGTG
NM_001347934.2:c.-92_-80delinsTGGAAGCAGAGTG	NP_001334863.1:n.-92_-80delinsTGGAAGCAGAGTG
NR_144940.2:n.276_288delinsTGGAAGCAGAGTG
NR_144941.2:n.276_288delinsTGGAAGCAGAGTG
NR_144942.2:n.276_288delinsTGGAAGCAGAGTG
NR_144943.2:n.276_288delinsTGGAAGCAGAGTG