Canonical Allele Identifier: CA1960356610
Gene: METTL15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.28212269C= , CM000673.2:g.28212269C= GRCh38
NC_000011.9:g.28233816C= , CM000673.1:g.28233816C= GRCh37
NC_000011.8:g.28190392C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000407364.8:c.407+1071C= MANE Select ENSP00000384369.3:n.407+1071C=
ENST00000303459.10:c.407+1071C= ENSP00000307251.6:n.407+1071C=
ENST00000406787.7:c.407+1071C= ENSP00000385507.3:n.407+1071C=
ENST00000407364.7:c.407+1071C= ENSP00000384369.3:n.407+1071C=
ENST00000451385.6:c.*21+1071C= ENSP00000396550.1:n.*21+1071C=
ENST00000532947.2:c.271-77937C= ENSP00000489497.1:n.271-77937C=
ENST00000634627.1:c.407+1071C= ENSP00000489381.1:n.407+1071C=
ENST00000634973.1:c.407+1071C= ENSP00000489505.1:n.407+1071C=
NM_001113528.1:c.407+1071C= NP_001107000.1:n.407+1071C=
NM_001297775.1:c.407+1071C= NP_001284704.1:n.407+1071C=
NM_152636.2:c.407+1071C= NP_689849.2:n.407+1071C=
XM_011519935.1:c.212+1071C= XP_011518237.1:n.212+1071C=
XM_011519936.1:c.212+1071C= XP_011518238.1:n.212+1071C=
XM_011519937.1:c.212+1071C= XP_011518239.1:n.212+1071C=
XM_011519938.1:c.-238+1071C= XP_011518240.1:n.-238+1071C=
XM_011519939.1:c.-78+1071C= XP_011518241.1:n.-78+1071C=
XM_011519940.1:c.407+1071C= XP_011518242.1:n.407+1071C=
XM_011519941.1:c.407+1071C= XP_011518243.1:n.407+1071C=
XR_930849.1:n.862+1071C=
XR_930850.1:n.862+1071C=
XM_011519935.3:c.212+1071C= XP_011518237.1:n.212+1071C=
XM_011519940.3:c.407+1071C= XP_011518242.1:n.407+1071C=
XM_011519941.2:c.407+1071C= XP_011518243.1:n.407+1071C=
XM_017017297.2:c.407+1071C= XP_016872786.1:n.407+1071C=
XM_017017300.2:c.125+1071C= XP_016872789.1:n.125+1071C=
XM_017017301.2:c.407+1071C= XP_016872790.1:n.407+1071C=
XM_017017303.2:c.-78+1071C= XP_016872792.1:n.-78+1071C=
XM_024448380.1:c.212+1071C= XP_024304148.1:n.212+1071C=
XM_024448381.1:c.212+1071C= XP_024304149.1:n.212+1071C=
XM_024448382.1:c.-238+1071C= XP_024304150.1:n.-238+1071C=
XR_001747787.1:n.534+1071C=
XR_930849.2:n.764+1071C=
NM_001113528.2:c.407+1071C= MANE Select NP_001107000.1:n.407+1071C=
NM_001297775.2:c.407+1071C= NP_001284704.1:n.407+1071C=
NM_152636.3:c.407+1071C= NP_689849.2:n.407+1071C=