Canonical Allele Identifier: CA2469916073

Gene: TBL1Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.7090124C= , CM000686.2:g.7090124C=	GRCh38
NC_000024.9:g.6958165C= , CM000686.1:g.6958165C=	GRCh37
NC_000024.8:g.7018165C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383032.6:c.1482C= MANE Select	ENSP00000372499.1:p.Gly494=
ENST00000651523.1:c.239C=
ENST00000346432.3:c.1482C=	ENSP00000328879.4:p.Gly494=
ENST00000355162.6:c.1482C=	ENSP00000347289.2:p.Gly494=
ENST00000383032.5:c.1482C=	ENSP00000372499.1:p.Gly494=
NM_033284.1:c.1482C=	NP_150600.1:p.Gly494=
NM_134258.1:c.1482C=	NP_599020.1:p.Gly494=
NM_134259.1:c.1482C=	NP_599021.1:p.Gly494=
XM_005262572.2:c.1524C=	XP_005262629.1:p.Gly508=
XM_005262572.3:c.1524C=	XP_005262629.1:p.Gly508=
XM_017030086.1:c.1482C=	XP_016885575.1:p.Gly494=
XM_017030087.1:c.1482C=	XP_016885576.1:p.Gly494=
XM_024452497.1:c.1482C=	XP_024308265.1:p.Gly494=
NM_033284.2:c.1482C= MANE Select	NP_150600.1:p.Gly494=
NM_134258.2:c.1482C=	NP_599020.1:p.Gly494=
NM_134259.2:c.1482C=	NP_599021.1:p.Gly494=