Canonical Allele Identifier: CA1138865386

Gene: TBL1Y

Linked Data

• gnomAD v3: Y-6993189-T-TTTCCTTTC
• gnomAD v4: Y-6993189-T-TTTCCTTTC

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.6993191_6993192insCCTTTCTT , CM000686.2:g.6993191_6993192insCCTTTCTT	GRCh38
NC_000024.9:g.6861232_6861233insCCTTTCTT , CM000686.1:g.6861232_6861233insCCTTTCTT	GRCh37
NC_000024.8:g.6921232_6921233insCCTTTCTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383032.6:c.-234-2613_-234-2612insCCTTTCTT MANE Select	ENSP00000372499.1:n.-234-2613_-234-2612insCCTTTCTT
ENST00000346432.3:c.-140+14948_-140+14949insCCTTTCTT	ENSP00000328879.4:n.-140+14948_-140+14949insCCTTTCTT
ENST00000355162.6:c.-234-2613_-234-2612insCCTTTCTT	ENSP00000347289.2:n.-234-2613_-234-2612insCCTTTCTT
ENST00000383032.5:c.-234-2613_-234-2612insCCTTTCTT	ENSP00000372499.1:n.-234-2613_-234-2612insCCTTTCTT
NM_033284.1:c.-234-2613_-234-2612insCCTTTCTT	NP_150600.1:n.-234-2613_-234-2612insCCTTTCTT
NM_134258.1:c.-234-2613_-234-2612insCCTTTCTT	NP_599020.1:n.-234-2613_-234-2612insCCTTTCTT
NM_134259.1:c.-140+14948_-140+14949insCCTTTCTT	NP_599021.1:n.-140+14948_-140+14949insCCTTTCTT
XM_017030086.1:c.-234-2613_-234-2612insCCTTTCTT	XP_016885575.1:n.-234-2613_-234-2612insCCTTTCTT
XM_017030087.1:c.-234-2613_-234-2612insCCTTTCTT	XP_016885576.1:n.-234-2613_-234-2612insCCTTTCTT
XM_024452497.1:c.-234-2613_-234-2612insCCTTTCTT	XP_024308265.1:n.-234-2613_-234-2612insCCTTTCTT
NM_033284.2:c.-234-2613_-234-2612insCCTTTCTT MANE Select	NP_150600.1:n.-234-2613_-234-2612insCCTTTCTT
NM_134258.2:c.-234-2613_-234-2612insCCTTTCTT	NP_599020.1:n.-234-2613_-234-2612insCCTTTCTT
NM_134259.2:c.-140+14948_-140+14949insCCTTTCTT	NP_599021.1:n.-140+14948_-140+14949insCCTTTCTT