Canonical Allele Identifier: CA2501476922

Gene: TBL1Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.6920185dup , CM000686.2:g.6920185dup	GRCh38
NC_000024.9:g.6788226dup , CM000686.1:g.6788226dup	GRCh37
NC_000024.8:g.6848226dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000383032.6:c.-266+8013dup MANE Select	ENSP00000372499.1:n.-266+8013dup
ENST00000346432.3:c.-171+8013dup	ENSP00000328879.4:n.-171+8013dup
ENST00000355162.6:c.-235+8013dup	ENSP00000347289.2:n.-235+8013dup
ENST00000383032.5:c.-266+8013dup	ENSP00000372499.1:n.-266+8013dup
NM_033284.1:c.-266+8013dup	NP_150600.1:n.-266+8013dup
NM_134258.1:c.-235+8013dup	NP_599020.1:n.-235+8013dup
NM_134259.1:c.-171+8013dup	NP_599021.1:n.-171+8013dup
XM_017030086.1:c.-266+8013dup	XP_016885575.1:n.-266+8013dup
XM_017030087.1:c.-266+8013dup	XP_016885576.1:n.-266+8013dup
XM_024452497.1:c.-266+8013dup	XP_024308265.1:n.-266+8013dup
NM_033284.2:c.-266+8013dup MANE Select	NP_150600.1:n.-266+8013dup
NM_134258.2:c.-235+8013dup	NP_599020.1:n.-235+8013dup
NM_134259.2:c.-171+8013dup	NP_599021.1:n.-171+8013dup