Canonical Allele Identifier: CA2469909927

Gene: TBL1Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.6985395_6985396delinsGT , CM000686.2:g.6985395_6985396delinsGT	GRCh38
NC_000024.9:g.6853436_6853437delinsGT , CM000686.1:g.6853436_6853437delinsGT	GRCh37
NC_000024.8:g.6913436_6913437delinsGT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383032.6:c.-235+7152_-235+7153delinsGT MANE Select	ENSP00000372499.1:n.-235+7152_-235+7153delinsGT
ENST00000346432.3:c.-140+7152_-140+7153delinsGT	ENSP00000328879.4:n.-140+7152_-140+7153delinsGT
ENST00000355162.6:c.-234-10409_-234-10408delinsGT	ENSP00000347289.2:n.-234-10409_-234-10408delinsGT
ENST00000383032.5:c.-235+7152_-235+7153delinsGT	ENSP00000372499.1:n.-235+7152_-235+7153delinsGT
NM_033284.1:c.-235+7152_-235+7153delinsGT	NP_150600.1:n.-235+7152_-235+7153delinsGT
NM_134258.1:c.-234-10409_-234-10408delinsGT	NP_599020.1:n.-234-10409_-234-10408delinsGT
NM_134259.1:c.-140+7152_-140+7153delinsGT	NP_599021.1:n.-140+7152_-140+7153delinsGT
XM_017030086.1:c.-235+7152_-235+7153delinsGT	XP_016885575.1:n.-235+7152_-235+7153delinsGT
XM_017030087.1:c.-235+7152_-235+7153delinsGT	XP_016885576.1:n.-235+7152_-235+7153delinsGT
XM_024452497.1:c.-235+7152_-235+7153delinsGT	XP_024308265.1:n.-235+7152_-235+7153delinsGT
NM_033284.2:c.-235+7152_-235+7153delinsGT MANE Select	NP_150600.1:n.-235+7152_-235+7153delinsGT
NM_134258.2:c.-234-10409_-234-10408delinsGT	NP_599020.1:n.-234-10409_-234-10408delinsGT
NM_134259.2:c.-140+7152_-140+7153delinsGT	NP_599021.1:n.-140+7152_-140+7153delinsGT