Canonical Allele Identifier: CA675197177

Gene: METTL15

Linked Data

• dbSNP Id: rs1184442571
• gnomAD v3: 11-28212277-C-T
• gnomAD v4: 11-28212277-C-T
• MyVariant Identifiers: chr11:g.28233824C>T (hg19) ; chr11:g.28212277C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.28212277C>T , CM000673.2:g.28212277C>T	GRCh38
NC_000011.9:g.28233824C>T , CM000673.1:g.28233824C>T	GRCh37
NC_000011.8:g.28190400C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000407364.8:c.407+1079C>T MANE Select	ENSP00000384369.3:n.407+1079C>T
ENST00000303459.10:c.407+1079C>T	ENSP00000307251.6:n.407+1079C>T
ENST00000406787.7:c.407+1079C>T	ENSP00000385507.3:n.407+1079C>T
ENST00000407364.7:c.407+1079C>T	ENSP00000384369.3:n.407+1079C>T
ENST00000451385.6:c.*21+1079C>T	ENSP00000396550.1:n.*21+1079C>T
ENST00000532947.2:c.271-77929C>T	ENSP00000489497.1:n.271-77929C>T
ENST00000634627.1:c.407+1079C>T	ENSP00000489381.1:n.407+1079C>T
ENST00000634973.1:c.407+1079C>T	ENSP00000489505.1:n.407+1079C>T
NM_001113528.1:c.407+1079C>T	NP_001107000.1:n.407+1079C>T
NM_001297775.1:c.407+1079C>T	NP_001284704.1:n.407+1079C>T
NM_152636.2:c.407+1079C>T	NP_689849.2:n.407+1079C>T
XM_011519935.1:c.212+1079C>T	XP_011518237.1:n.212+1079C>T
XM_011519936.1:c.212+1079C>T	XP_011518238.1:n.212+1079C>T
XM_011519937.1:c.212+1079C>T	XP_011518239.1:n.212+1079C>T
XM_011519938.1:c.-238+1079C>T	XP_011518240.1:n.-238+1079C>T
XM_011519939.1:c.-78+1079C>T	XP_011518241.1:n.-78+1079C>T
XM_011519940.1:c.407+1079C>T	XP_011518242.1:n.407+1079C>T
XM_011519941.1:c.407+1079C>T	XP_011518243.1:n.407+1079C>T
XR_930849.1:n.862+1079C>T
XR_930850.1:n.862+1079C>T
XM_011519935.3:c.212+1079C>T	XP_011518237.1:n.212+1079C>T
XM_011519940.3:c.407+1079C>T	XP_011518242.1:n.407+1079C>T
XM_011519941.2:c.407+1079C>T	XP_011518243.1:n.407+1079C>T
XM_017017297.2:c.407+1079C>T	XP_016872786.1:n.407+1079C>T
XM_017017300.2:c.125+1079C>T	XP_016872789.1:n.125+1079C>T
XM_017017301.2:c.407+1079C>T	XP_016872790.1:n.407+1079C>T
XM_017017303.2:c.-78+1079C>T	XP_016872792.1:n.-78+1079C>T
XM_024448380.1:c.212+1079C>T	XP_024304148.1:n.212+1079C>T
XM_024448381.1:c.212+1079C>T	XP_024304149.1:n.212+1079C>T
XM_024448382.1:c.-238+1079C>T	XP_024304150.1:n.-238+1079C>T
XR_001747787.1:n.534+1079C>T
XR_930849.2:n.764+1079C>T
NM_001113528.2:c.407+1079C>T MANE Select	NP_001107000.1:n.407+1079C>T
NM_001297775.2:c.407+1079C>T	NP_001284704.1:n.407+1079C>T
NM_152636.3:c.407+1079C>T	NP_689849.2:n.407+1079C>T