Canonical Allele Identifier: CA2469914554

Gene: TBL1Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.7064742G= , CM000686.2:g.7064742G=	GRCh38
NC_000024.9:g.6932783G= , CM000686.1:g.6932783G=	GRCh37
NC_000024.8:g.6992783G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000383032.6:c.457+593G= MANE Select	ENSP00000372499.1:n.457+593G=
ENST00000346432.3:c.457+593G=	ENSP00000328879.4:n.457+593G=
ENST00000355162.6:c.457+593G=	ENSP00000347289.2:n.457+593G=
ENST00000383032.5:c.457+593G=	ENSP00000372499.1:n.457+593G=
NM_033284.1:c.457+593G=	NP_150600.1:n.457+593G=
NM_134258.1:c.457+593G=	NP_599020.1:n.457+593G=
NM_134259.1:c.457+593G=	NP_599021.1:n.457+593G=
XM_005262572.2:c.499+593G=	XP_005262629.1:n.499+593G=
XM_005262572.3:c.499+593G=	XP_005262629.1:n.499+593G=
XM_017030086.1:c.457+593G=	XP_016885575.1:n.457+593G=
XM_017030087.1:c.457+593G=	XP_016885576.1:n.457+593G=
XM_024452497.1:c.457+593G=	XP_024308265.1:n.457+593G=
NM_033284.2:c.457+593G= MANE Select	NP_150600.1:n.457+593G=
NM_134258.2:c.457+593G=	NP_599020.1:n.457+593G=
NM_134259.2:c.457+593G=	NP_599021.1:n.457+593G=