Canonical Allele Identifier: CA1110926116

Gene: TRMT9B

Linked Data

• dbSNP Id: rs1800938706
• gnomAD v3: 8-12953708-GTAA-G
• gnomAD v4: 8-12953708-GTAA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.12953709_12953711del , CM000670.2:g.12953709_12953711del	GRCh38
NC_000008.10:g.12811218_12811220del , CM000670.1:g.12811218_12811220del	GRCh37
NC_000008.9:g.12855589_12855591del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528335.6:c.-200+1351_-200+1353del	ENSP00000518785.1:n.-200+1351_-200+1353del
ENST00000524591.7:c.-200+7743_-200+7745del MANE Select	ENSP00000432695.1:n.-200+7743_-200+7745del
ENST00000400069.7:c.-169+1351_-169+1353del	ENSP00000468715.1:n.-169+1351_-169+1353del
ENST00000447063.6:c.-200+7743_-200+7745del	ENSP00000443288.1:n.-200+7743_-200+7745del
ENST00000524591.6:c.-200+7743_-200+7745del	ENSP00000432695.1:n.-200+7743_-200+7745del
ENST00000525249.1:n.293+7743_293+7745del
ENST00000528335.5:n.349+1351_349+1353del
ENST00000528753.2:c.-200+1351_-200+1353del	ENSP00000466330.1:n.-200+1351_-200+1353del
ENST00000532376.2:c.-169+1351_-169+1353del	ENSP00000431717.2:n.-169+1351_-169+1353del
NM_020844.2:c.-200+7743_-200+7745del	NP_065895.2:n.-200+7743_-200+7745del
XM_005273584.3:c.39+1005_39+1007del	XP_005273641.1:n.39+1005_39+1007del
XM_005273585.3:c.-109+1351_-109+1353del	XP_005273642.1:n.-109+1351_-109+1353del
XM_005273586.3:c.-200+1351_-200+1353del	XP_005273643.1:n.-200+1351_-200+1353del
XM_011544596.1:c.254+1351_254+1353del	XP_011542898.1:n.254+1351_254+1353del
XM_011544597.1:c.254+1351_254+1353del	XP_011542899.1:n.254+1351_254+1353del
XM_011544598.1:c.-109+1351_-109+1353del	XP_011542900.1:n.-109+1351_-109+1353del
XM_011544599.1:c.-1984-892_-1984-890del	XP_011542901.1:n.-1984-892_-1984-890del
XM_011544601.1:c.-109+7743_-109+7745del	XP_011542903.1:n.-109+7743_-109+7745del
XM_005273584.5:c.39+1005_39+1007del	XP_005273641.1:n.39+1005_39+1007del
XM_005273585.4:c.-109+1351_-109+1353del	XP_005273642.1:n.-109+1351_-109+1353del
XM_005273586.4:c.-200+1351_-200+1353del	XP_005273643.1:n.-200+1351_-200+1353del
XM_005273588.5:c.-378+1351_-378+1353del	XP_005273645.1:n.-378+1351_-378+1353del
XM_005273591.5:c.-409+1351_-409+1353del	XP_005273648.1:n.-409+1351_-409+1353del
XM_011544596.3:c.254+1351_254+1353del	XP_011542898.1:n.254+1351_254+1353del
XM_011544597.3:c.254+1351_254+1353del	XP_011542899.1:n.254+1351_254+1353del
XM_011544598.2:c.-109+1351_-109+1353del	XP_011542900.1:n.-109+1351_-109+1353del
XM_011544601.3:c.-109+7743_-109+7745del	XP_011542903.1:n.-109+7743_-109+7745del
XM_017013706.2:c.-200+1005_-200+1007del	XP_016869195.1:n.-200+1005_-200+1007del
XM_017013710.1:c.-434+1351_-434+1353del	XP_016869199.1:n.-434+1351_-434+1353del
XM_017013714.2:c.-306+1351_-306+1353del	XP_016869203.1:n.-306+1351_-306+1353del
XM_024447214.1:c.-263+1351_-263+1353del	XP_024302982.1:n.-263+1351_-263+1353del
XM_024447215.1:c.-354+1351_-354+1353del	XP_024302983.1:n.-354+1351_-354+1353del
XM_024447216.1:c.-378+1351_-378+1353del	XP_024302984.1:n.-378+1351_-378+1353del
XM_024447219.1:c.-1098+1351_-1098+1353del	XP_024302987.1:n.-1098+1351_-1098+1353del
NM_020844.3:c.-200+7743_-200+7745del MANE Select	NP_065895.2:n.-200+7743_-200+7745del