Canonical Allele Identifier: CA414969864

Gene: TBL1Y

Linked Data

• MyVariant Identifiers: chrY:g.6938835G>C (hg19) ; chrY:g.7070794G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.7070794G>C , CM000686.2:g.7070794G>C	GRCh38
NC_000024.9:g.6938835G>C , CM000686.1:g.6938835G>C	GRCh37
NC_000024.8:g.6998835G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383032.6:c.665G>C MANE Select	ENSP00000372499.1:p.Arg222Thr
ENST00000346432.3:c.665G>C	ENSP00000328879.4:p.Arg222Thr
ENST00000355162.6:c.665G>C	ENSP00000347289.2:p.Arg222Thr
ENST00000383032.5:c.665G>C	ENSP00000372499.1:p.Arg222Thr
NM_033284.1:c.665G>C	NP_150600.1:p.Arg222Thr
NM_134258.1:c.665G>C	NP_599020.1:p.Arg222Thr
NM_134259.1:c.665G>C	NP_599021.1:p.Arg222Thr
XM_005262572.2:c.707G>C	XP_005262629.1:p.Arg236Thr
XM_005262572.3:c.707G>C	XP_005262629.1:p.Arg236Thr
XM_017030086.1:c.665G>C	XP_016885575.1:p.Arg222Thr
XM_017030087.1:c.665G>C	XP_016885576.1:p.Arg222Thr
XM_024452497.1:c.665G>C	XP_024308265.1:p.Arg222Thr
NM_033284.2:c.665G>C MANE Select	NP_150600.1:p.Arg222Thr
NM_134258.2:c.665G>C	NP_599020.1:p.Arg222Thr
NM_134259.2:c.665G>C	NP_599021.1:p.Arg222Thr