Canonical Allele Identifier: CA414970019
Gene: TBL1Y HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.7070859A>T , CM000686.2:g.7070859A>T GRCh38
NC_000024.9:g.6938900A>T , CM000686.1:g.6938900A>T GRCh37
NC_000024.8:g.6998900A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000383032.6:c.730A>T MANE Select ENSP00000372499.1:p.Asn244Tyr
ENST00000346432.3:c.730A>T ENSP00000328879.4:p.Asn244Tyr
ENST00000355162.6:c.730A>T ENSP00000347289.2:p.Asn244Tyr
ENST00000383032.5:c.730A>T ENSP00000372499.1:p.Asn244Tyr
NM_033284.1:c.730A>T NP_150600.1:p.Asn244Tyr
NM_134258.1:c.730A>T NP_599020.1:p.Asn244Tyr
NM_134259.1:c.730A>T NP_599021.1:p.Asn244Tyr
XM_005262572.2:c.772A>T XP_005262629.1:p.Asn258Tyr
XM_005262572.3:c.772A>T XP_005262629.1:p.Asn258Tyr
XM_017030086.1:c.730A>T XP_016885575.1:p.Asn244Tyr
XM_017030087.1:c.730A>T XP_016885576.1:p.Asn244Tyr
XM_024452497.1:c.730A>T XP_024308265.1:p.Asn244Tyr
NM_033284.2:c.730A>T MANE Select NP_150600.1:p.Asn244Tyr
NM_134258.2:c.730A>T NP_599020.1:p.Asn244Tyr
NM_134259.2:c.730A>T NP_599021.1:p.Asn244Tyr