Canonical Allele Identifier: CA2593019466

Gene: TRMT9B

Linked Data

• gnomAD v3: 8-12953539-A-AGG
• gnomAD v4: 8-12953539-A-AGG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.12953543_12953544dup , CM000670.2:g.12953543_12953544dup	GRCh38
NC_000008.10:g.12811052_12811053dup , CM000670.1:g.12811052_12811053dup	GRCh37
NC_000008.9:g.12855423_12855424dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528335.6:c.-200+1185_-200+1186dup	ENSP00000518785.1:n.-200+1185_-200+1186dup
ENST00000524591.7:c.-200+7577_-200+7578dup MANE Select	ENSP00000432695.1:n.-200+7577_-200+7578dup
ENST00000400069.7:c.-169+1185_-169+1186dup	ENSP00000468715.1:n.-169+1185_-169+1186dup
ENST00000447063.6:c.-200+7577_-200+7578dup	ENSP00000443288.1:n.-200+7577_-200+7578dup
ENST00000524591.6:c.-200+7577_-200+7578dup	ENSP00000432695.1:n.-200+7577_-200+7578dup
ENST00000525249.1:n.293+7577_293+7578dup
ENST00000528335.5:n.349+1185_349+1186dup
ENST00000528753.2:c.-200+1185_-200+1186dup	ENSP00000466330.1:n.-200+1185_-200+1186dup
ENST00000532376.2:c.-169+1185_-169+1186dup	ENSP00000431717.2:n.-169+1185_-169+1186dup
NM_020844.2:c.-200+7577_-200+7578dup	NP_065895.2:n.-200+7577_-200+7578dup
XM_005273584.3:c.39+839_39+840dup	XP_005273641.1:n.39+839_39+840dup
XM_005273585.3:c.-109+1185_-109+1186dup	XP_005273642.1:n.-109+1185_-109+1186dup
XM_005273586.3:c.-200+1185_-200+1186dup	XP_005273643.1:n.-200+1185_-200+1186dup
XM_011544596.1:c.254+1185_254+1186dup	XP_011542898.1:n.254+1185_254+1186dup
XM_011544597.1:c.254+1185_254+1186dup	XP_011542899.1:n.254+1185_254+1186dup
XM_011544598.1:c.-109+1185_-109+1186dup	XP_011542900.1:n.-109+1185_-109+1186dup
XM_011544599.1:c.-1984-1058_-1984-1057dup	XP_011542901.1:n.-1984-1058_-1984-1057dup
XM_011544601.1:c.-109+7577_-109+7578dup	XP_011542903.1:n.-109+7577_-109+7578dup
XM_005273584.5:c.39+839_39+840dup	XP_005273641.1:n.39+839_39+840dup
XM_005273585.4:c.-109+1185_-109+1186dup	XP_005273642.1:n.-109+1185_-109+1186dup
XM_005273586.4:c.-200+1185_-200+1186dup	XP_005273643.1:n.-200+1185_-200+1186dup
XM_005273588.5:c.-378+1185_-378+1186dup	XP_005273645.1:n.-378+1185_-378+1186dup
XM_005273591.5:c.-409+1185_-409+1186dup	XP_005273648.1:n.-409+1185_-409+1186dup
XM_011544596.3:c.254+1185_254+1186dup	XP_011542898.1:n.254+1185_254+1186dup
XM_011544597.3:c.254+1185_254+1186dup	XP_011542899.1:n.254+1185_254+1186dup
XM_011544598.2:c.-109+1185_-109+1186dup	XP_011542900.1:n.-109+1185_-109+1186dup
XM_011544601.3:c.-109+7577_-109+7578dup	XP_011542903.1:n.-109+7577_-109+7578dup
XM_017013706.2:c.-200+839_-200+840dup	XP_016869195.1:n.-200+839_-200+840dup
XM_017013710.1:c.-434+1185_-434+1186dup	XP_016869199.1:n.-434+1185_-434+1186dup
XM_017013714.2:c.-306+1185_-306+1186dup	XP_016869203.1:n.-306+1185_-306+1186dup
XM_024447214.1:c.-263+1185_-263+1186dup	XP_024302982.1:n.-263+1185_-263+1186dup
XM_024447215.1:c.-354+1185_-354+1186dup	XP_024302983.1:n.-354+1185_-354+1186dup
XM_024447216.1:c.-378+1185_-378+1186dup	XP_024302984.1:n.-378+1185_-378+1186dup
XM_024447219.1:c.-1098+1185_-1098+1186dup	XP_024302987.1:n.-1098+1185_-1098+1186dup
NM_020844.3:c.-200+7577_-200+7578dup MANE Select	NP_065895.2:n.-200+7577_-200+7578dup