Canonical Allele Identifier: CA1138865414

Gene: TBL1Y

Linked Data

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

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.6993193_6993194insCTTCTTTC , CM000686.2:g.6993193_6993194insCTTCTTTC	GRCh38
NC_000024.9:g.6861234_6861235insCTTCTTTC , CM000686.1:g.6861234_6861235insCTTCTTTC	GRCh37
NC_000024.8:g.6921234_6921235insCTTCTTTC	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000383032.6:c.-234-2611_-234-2610insCTTCTTTC MANE Select	ENSP00000372499.1:n.-234-2611_-234-2610insCTTCTTTC
ENST00000346432.3:c.-140+14950_-140+14951insCTTCTTTC	ENSP00000328879.4:n.-140+14950_-140+14951insCTTCTTTC
ENST00000355162.6:c.-234-2611_-234-2610insCTTCTTTC	ENSP00000347289.2:n.-234-2611_-234-2610insCTTCTTTC
ENST00000383032.5:c.-234-2611_-234-2610insCTTCTTTC	ENSP00000372499.1:n.-234-2611_-234-2610insCTTCTTTC
NM_033284.1:c.-234-2611_-234-2610insCTTCTTTC	NP_150600.1:n.-234-2611_-234-2610insCTTCTTTC
NM_134258.1:c.-234-2611_-234-2610insCTTCTTTC	NP_599020.1:n.-234-2611_-234-2610insCTTCTTTC
NM_134259.1:c.-140+14950_-140+14951insCTTCTTTC	NP_599021.1:n.-140+14950_-140+14951insCTTCTTTC
XM_017030086.1:c.-234-2611_-234-2610insCTTCTTTC	XP_016885575.1:n.-234-2611_-234-2610insCTTCTTTC
XM_017030087.1:c.-234-2611_-234-2610insCTTCTTTC	XP_016885576.1:n.-234-2611_-234-2610insCTTCTTTC
XM_024452497.1:c.-234-2611_-234-2610insCTTCTTTC	XP_024308265.1:n.-234-2611_-234-2610insCTTCTTTC
NM_033284.2:c.-234-2611_-234-2610insCTTCTTTC MANE Select	NP_150600.1:n.-234-2611_-234-2610insCTTCTTTC
NM_134258.2:c.-234-2611_-234-2610insCTTCTTTC	NP_599020.1:n.-234-2611_-234-2610insCTTCTTTC
NM_134259.2:c.-140+14950_-140+14951insCTTCTTTC	NP_599021.1:n.-140+14950_-140+14951insCTTCTTTC