Canonical Allele Identifier: CA64882675

Gene: METTL21A

Linked Data

• dbSNP Id: rs1022551962
• gnomAD v2: 2-208473026-C-CT
• gnomAD v3: 2-207608302-C-CT
• gnomAD v4: 2-207608302-C-CT
• MyVariant Identifiers: chr2:g.208473026_208473027insT (hg19) ; chr2:g.207608302_207608303insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.207608302_207608303insT , CM000664.2:g.207608302_207608303insT	GRCh38
NC_000002.11:g.208473026_208473027insT , CM000664.1:g.208473026_208473027insT	GRCh37
NC_000002.10:g.208181271_208181272insT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000425132.5:c.259+13503_259+13504insA	ENSP00000400730.1:n.259+13503_259+13504in...
ENST00000432416.5:c.259+13503_259+13504insA	ENSP00000416570.1:n.259+13503_259+13504in...
ENST00000458426.5:c.259+13503_259+13504insA	ENSP00000389684.1:n.259+13503_259+13504in...
NM_001308021.1:c.259+13503_259+13504insA	NP_001294950.1:n.259+13503_259+13504insA
XM_011510727.1:c.334+13503_334+13504insA	XP_011509029.1:n.334+13503_334+13504insA
XM_011510728.1:c.334+13503_334+13504insA	XP_011509030.1:n.334+13503_334+13504insA
XM_011510729.1:c.388+12338_388+12339insA	XP_011509031.1:n.388+12338_388+12339insA
NM_001308021.2:c.259+13503_259+13504insA	NP_001294950.1:n.259+13503_259+13504insA
NM_001330131.1:c.259+13503_259+13504insA	NP_001317060.1:n.259+13503_259+13504insA
NM_001330132.1:c.259+13503_259+13504insA	NP_001317061.1:n.259+13503_259+13504insA
NM_001330133.1:c.259+13503_259+13504insA	NP_001317062.1:n.259+13503_259+13504insA
NM_001330135.1:c.259+13503_259+13504insA	NP_001317064.1:n.259+13503_259+13504insA
NM_001330136.1:c.259+13503_259+13504insA	NP_001317065.1:n.259+13503_259+13504insA
XM_011510727.3:c.334+13503_334+13504insA	XP_011509029.1:n.334+13503_334+13504insA
XM_011510728.3:c.334+13503_334+13504insA	XP_011509030.1:n.334+13503_334+13504insA
XM_011510729.2:c.388+12338_388+12339insA	XP_011509031.1:n.388+12338_388+12339insA
XM_017003445.1:c.334+13503_334+13504insA	XP_016858934.1:n.334+13503_334+13504insA
XM_024452724.1:c.259+13503_259+13504insA	XP_024308492.1:n.259+13503_259+13504insA
XM_024452725.1:c.259+13503_259+13504insA	XP_024308493.1:n.259+13503_259+13504insA
XM_024452726.1:c.313+12338_313+12339insA	XP_024308494.1:n.313+12338_313+12339insA
NM_001308021.3:c.259+13503_259+13504insA	NP_001294950.1:n.259+13503_259+13504insA
NM_001330131.2:c.259+13503_259+13504insA	NP_001317060.1:n.259+13503_259+13504insA
NM_001330135.2:c.259+13503_259+13504insA	NP_001317064.1:n.259+13503_259+13504insA
NM_001330132.3:c.259+13503_259+13504insA	NP_001317061.1:n.259+13503_259+13504insA
NM_001330133.3:c.259+13503_259+13504insA	NP_001317062.1:n.259+13503_259+13504insA
NM_001330136.3:c.259+13503_259+13504insA	NP_001317065.1:n.259+13503_259+13504insA
NM_001388427.1:c.259+13503_259+13504insA	NP_001375356.1:n.259+13503_259+13504insA
NM_001388439.2:c.259+13503_259+13504insA	NP_001375368.1:n.259+13503_259+13504insA
NM_001393563.1:c.313+12338_313+12339insA	NP_001380492.1:n.313+12338_313+12339insA
NM_001393564.1:c.259+13503_259+13504insA	NP_001380493.1:n.259+13503_259+13504insA
NM_001393565.1:c.259+13503_259+13504insA	NP_001380494.1:n.259+13503_259+13504insA
NM_001393566.1:c.259+13503_259+13504insA	NP_001380495.1:n.259+13503_259+13504insA
NM_001393567.1:c.259+13503_259+13504insA	NP_001380496.1:n.259+13503_259+13504insA
NM_001393568.1:c.314-11189_314-11188insA	NP_001380497.1:n.314-11189_314-11188insA
NM_001393569.1:c.313+12338_313+12339insA	NP_001380498.1:n.313+12338_313+12339insA
NM_001393570.1:c.313+12338_313+12339insA	NP_001380499.1:n.313+12338_313+12339insA
NM_001393571.1:c.260-11189_260-11188insA	NP_001380500.1:n.260-11189_260-11188insA
NM_001393572.1:c.260-11189_260-11188insA	NP_001380501.1:n.260-11189_260-11188insA
NM_001393573.1:c.259+13503_259+13504insA	NP_001380502.1:n.259+13503_259+13504insA
NM_001393574.1:c.259+13503_259+13504insA	NP_001380503.1:n.259+13503_259+13504insA
NM_001393575.1:c.259+13503_259+13504insA	NP_001380504.1:n.259+13503_259+13504insA