Canonical Allele Identifier: CA645286382

Gene: TBL1Y

Linked Data

• dbSNP Id: rs1174754908
• gnomAD v2: Y-6938911-C-A
• MyVariant Identifiers: chrY:g.6938911C>A (hg19) ; chrY:g.7070870C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.7070870C>A , CM000686.2:g.7070870C>A	GRCh38
NC_000024.9:g.6938911C>A , CM000686.1:g.6938911C>A	GRCh37
NC_000024.8:g.6998911C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383032.6:c.732+9C>A MANE Select	ENSP00000372499.1:n.732+9C>A
ENST00000346432.3:c.732+9C>A	ENSP00000328879.4:n.732+9C>A
ENST00000355162.6:c.732+9C>A	ENSP00000347289.2:n.732+9C>A
ENST00000383032.5:c.732+9C>A	ENSP00000372499.1:n.732+9C>A
NM_033284.1:c.732+9C>A	NP_150600.1:n.732+9C>A
NM_134258.1:c.732+9C>A	NP_599020.1:n.732+9C>A
NM_134259.1:c.732+9C>A	NP_599021.1:n.732+9C>A
XM_005262572.2:c.774+9C>A	XP_005262629.1:n.774+9C>A
XM_005262572.3:c.774+9C>A	XP_005262629.1:n.774+9C>A
XM_017030086.1:c.732+9C>A	XP_016885575.1:n.732+9C>A
XM_017030087.1:c.732+9C>A	XP_016885576.1:n.732+9C>A
XM_024452497.1:c.732+9C>A	XP_024308265.1:n.732+9C>A
NM_033284.2:c.732+9C>A MANE Select	NP_150600.1:n.732+9C>A
NM_134258.2:c.732+9C>A	NP_599020.1:n.732+9C>A
NM_134259.2:c.732+9C>A	NP_599021.1:n.732+9C>A