Canonical Allele Identifier: CA598244735

Gene: METTL15

Linked Data

• dbSNP Id: rs1359368957
• gnomAD v2: 11-28233708-CTT-C
• gnomAD v3: 11-28212161-CTT-C
• gnomAD v4: 11-28212161-CTT-C
• MyVariant Identifiers: chr11:g.28233709_28233710del (hg19) ; chr11:g.28212162_28212163del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.28212163_28212164del , CM000673.2:g.28212163_28212164del	GRCh38
NC_000011.9:g.28233710_28233711del , CM000673.1:g.28233710_28233711del	GRCh37
NC_000011.8:g.28190286_28190287del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000407364.8:c.407+965_407+966del MANE Select	ENSP00000384369.3:n.407+965_407+966del
ENST00000303459.10:c.407+965_407+966del	ENSP00000307251.6:n.407+965_407+966del
ENST00000406787.7:c.407+965_407+966del	ENSP00000385507.3:n.407+965_407+966del
ENST00000407364.7:c.407+965_407+966del	ENSP00000384369.3:n.407+965_407+966del
ENST00000451385.6:c.*21+965_*21+966del	ENSP00000396550.1:n.*21+965_*21+966del
ENST00000532947.2:c.271-78043_271-78042del	ENSP00000489497.1:n.271-78043_271-78042de...
ENST00000634627.1:c.407+965_407+966del	ENSP00000489381.1:n.407+965_407+966del
ENST00000634973.1:c.407+965_407+966del	ENSP00000489505.1:n.407+965_407+966del
NM_001113528.1:c.407+965_407+966del	NP_001107000.1:n.407+965_407+966del
NM_001297775.1:c.407+965_407+966del	NP_001284704.1:n.407+965_407+966del
NM_152636.2:c.407+965_407+966del	NP_689849.2:n.407+965_407+966del
XM_011519935.1:c.212+965_212+966del	XP_011518237.1:n.212+965_212+966del
XM_011519936.1:c.212+965_212+966del	XP_011518238.1:n.212+965_212+966del
XM_011519937.1:c.212+965_212+966del	XP_011518239.1:n.212+965_212+966del
XM_011519938.1:c.-238+965_-238+966del	XP_011518240.1:n.-238+965_-238+966del
XM_011519939.1:c.-78+965_-78+966del	XP_011518241.1:n.-78+965_-78+966del
XM_011519940.1:c.407+965_407+966del	XP_011518242.1:n.407+965_407+966del
XM_011519941.1:c.407+965_407+966del	XP_011518243.1:n.407+965_407+966del
XR_930849.1:n.862+965_862+966del
XR_930850.1:n.862+965_862+966del
XM_011519935.3:c.212+965_212+966del	XP_011518237.1:n.212+965_212+966del
XM_011519940.3:c.407+965_407+966del	XP_011518242.1:n.407+965_407+966del
XM_011519941.2:c.407+965_407+966del	XP_011518243.1:n.407+965_407+966del
XM_017017297.2:c.407+965_407+966del	XP_016872786.1:n.407+965_407+966del
XM_017017300.2:c.125+965_125+966del	XP_016872789.1:n.125+965_125+966del
XM_017017301.2:c.407+965_407+966del	XP_016872790.1:n.407+965_407+966del
XM_017017303.2:c.-78+965_-78+966del	XP_016872792.1:n.-78+965_-78+966del
XM_024448380.1:c.212+965_212+966del	XP_024304148.1:n.212+965_212+966del
XM_024448381.1:c.212+965_212+966del	XP_024304149.1:n.212+965_212+966del
XM_024448382.1:c.-238+965_-238+966del	XP_024304150.1:n.-238+965_-238+966del
XR_001747787.1:n.534+965_534+966del
XR_930849.2:n.764+965_764+966del
NM_001113528.2:c.407+965_407+966del MANE Select	NP_001107000.1:n.407+965_407+966del
NM_001297775.2:c.407+965_407+966del	NP_001284704.1:n.407+965_407+966del
NM_152636.3:c.407+965_407+966del	NP_689849.2:n.407+965_407+966del