Canonical Allele Identifier: CA2589275531

Gene: TBL1Y

Linked Data

• gnomAD v3: Y-7073172-A-G
• gnomAD v4: Y-7073172-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.7073172A>G , CM000686.2:g.7073172A>G	GRCh38
NC_000024.9:g.6941213A>G , CM000686.1:g.6941213A>G	GRCh37
NC_000024.8:g.7001213A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383032.6:c.894+1342A>G MANE Select	ENSP00000372499.1:n.894+1342A>G
ENST00000346432.3:c.894+1342A>G	ENSP00000328879.4:n.894+1342A>G
ENST00000355162.6:c.894+1342A>G	ENSP00000347289.2:n.894+1342A>G
ENST00000383032.5:c.894+1342A>G	ENSP00000372499.1:n.894+1342A>G
NM_033284.1:c.894+1342A>G	NP_150600.1:n.894+1342A>G
NM_134258.1:c.894+1342A>G	NP_599020.1:n.894+1342A>G
NM_134259.1:c.894+1342A>G	NP_599021.1:n.894+1342A>G
XM_005262572.2:c.936+1342A>G	XP_005262629.1:n.936+1342A>G
XM_005262572.3:c.936+1342A>G	XP_005262629.1:n.936+1342A>G
XM_017030086.1:c.894+1342A>G	XP_016885575.1:n.894+1342A>G
XM_017030087.1:c.894+1342A>G	XP_016885576.1:n.894+1342A>G
XM_024452497.1:c.894+1342A>G	XP_024308265.1:n.894+1342A>G
NM_033284.2:c.894+1342A>G MANE Select	NP_150600.1:n.894+1342A>G
NM_134258.2:c.894+1342A>G	NP_599020.1:n.894+1342A>G
NM_134259.2:c.894+1342A>G	NP_599021.1:n.894+1342A>G