Canonical Allele Identifier: CA1138814390

Gene: TBL1Y

Linked Data

• gnomAD v3: Y-7070898-G-T
• gnomAD v4: Y-7070898-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.7070898G>T , CM000686.2:g.7070898G>T	GRCh38
NC_000024.9:g.6938939G>T , CM000686.1:g.6938939G>T	GRCh37
NC_000024.8:g.6998939G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383032.6:c.732+37G>T MANE Select	ENSP00000372499.1:n.732+37G>T
ENST00000346432.3:c.732+37G>T	ENSP00000328879.4:n.732+37G>T
ENST00000355162.6:c.732+37G>T	ENSP00000347289.2:n.732+37G>T
ENST00000383032.5:c.732+37G>T	ENSP00000372499.1:n.732+37G>T
NM_033284.1:c.732+37G>T	NP_150600.1:n.732+37G>T
NM_134258.1:c.732+37G>T	NP_599020.1:n.732+37G>T
NM_134259.1:c.732+37G>T	NP_599021.1:n.732+37G>T
XM_005262572.2:c.774+37G>T	XP_005262629.1:n.774+37G>T
XM_005262572.3:c.774+37G>T	XP_005262629.1:n.774+37G>T
XM_017030086.1:c.732+37G>T	XP_016885575.1:n.732+37G>T
XM_017030087.1:c.732+37G>T	XP_016885576.1:n.732+37G>T
XM_024452497.1:c.732+37G>T	XP_024308265.1:n.732+37G>T
NM_033284.2:c.732+37G>T MANE Select	NP_150600.1:n.732+37G>T
NM_134258.2:c.732+37G>T	NP_599020.1:n.732+37G>T
NM_134259.2:c.732+37G>T	NP_599021.1:n.732+37G>T