Canonical Allele Identifier: CA2469909923
Gene: TBL1Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.6985230C= , CM000686.2:g.6985230C= GRCh38
NC_000024.9:g.6853271C= , CM000686.1:g.6853271C= GRCh37
NC_000024.8:g.6913271C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000383032.6:c.-235+6987C= MANE Select ENSP00000372499.1:n.-235+6987C=
ENST00000346432.3:c.-140+6987C= ENSP00000328879.4:n.-140+6987C=
ENST00000355162.6:c.-234-10574C= ENSP00000347289.2:n.-234-10574C=
ENST00000383032.5:c.-235+6987C= ENSP00000372499.1:n.-235+6987C=
NM_033284.1:c.-235+6987C= NP_150600.1:n.-235+6987C=
NM_134258.1:c.-234-10574C= NP_599020.1:n.-234-10574C=
NM_134259.1:c.-140+6987C= NP_599021.1:n.-140+6987C=
XM_017030086.1:c.-235+6987C= XP_016885575.1:n.-235+6987C=
XM_017030087.1:c.-235+6987C= XP_016885576.1:n.-235+6987C=
XM_024452497.1:c.-235+6987C= XP_024308265.1:n.-235+6987C=
NM_033284.2:c.-235+6987C= MANE Select NP_150600.1:n.-235+6987C=
NM_134258.2:c.-234-10574C= NP_599020.1:n.-234-10574C=
NM_134259.2:c.-140+6987C= NP_599021.1:n.-140+6987C=