Canonical Allele Identifier: CA2469910293

Gene: TBL1Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.6991467A= , CM000686.2:g.6991467A=	GRCh38
NC_000024.9:g.6859508A= , CM000686.1:g.6859508A=	GRCh37
NC_000024.8:g.6919508A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383032.6:c.-234-4337A= MANE Select	ENSP00000372499.1:n.-234-4337A=
ENST00000346432.3:c.-140+13224A=	ENSP00000328879.4:n.-140+13224A=
ENST00000355162.6:c.-234-4337A=	ENSP00000347289.2:n.-234-4337A=
ENST00000383032.5:c.-234-4337A=	ENSP00000372499.1:n.-234-4337A=
NM_033284.1:c.-234-4337A=	NP_150600.1:n.-234-4337A=
NM_134258.1:c.-234-4337A=	NP_599020.1:n.-234-4337A=
NM_134259.1:c.-140+13224A=	NP_599021.1:n.-140+13224A=
XM_017030086.1:c.-234-4337A=	XP_016885575.1:n.-234-4337A=
XM_017030087.1:c.-234-4337A=	XP_016885576.1:n.-234-4337A=
XM_024452497.1:c.-234-4337A=	XP_024308265.1:n.-234-4337A=
NM_033284.2:c.-234-4337A= MANE Select	NP_150600.1:n.-234-4337A=
NM_134258.2:c.-234-4337A=	NP_599020.1:n.-234-4337A=
NM_134259.2:c.-140+13224A=	NP_599021.1:n.-140+13224A=