Canonical Allele Identifier: CA645286384

Gene: TBL1Y

Linked Data

• dbSNP Id: rs1380173326
• gnomAD v2: Y-6938944-A-C
• MyVariant Identifiers: chrY:g.6938944A>C (hg19) ; chrY:g.7070903A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.7070903A>C , CM000686.2:g.7070903A>C	GRCh38
NC_000024.9:g.6938944A>C , CM000686.1:g.6938944A>C	GRCh37
NC_000024.8:g.6998944A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383032.6:c.732+42A>C MANE Select	ENSP00000372499.1:n.732+42A>C
ENST00000346432.3:c.732+42A>C	ENSP00000328879.4:n.732+42A>C
ENST00000355162.6:c.732+42A>C	ENSP00000347289.2:n.732+42A>C
ENST00000383032.5:c.732+42A>C	ENSP00000372499.1:n.732+42A>C
NM_033284.1:c.732+42A>C	NP_150600.1:n.732+42A>C
NM_134258.1:c.732+42A>C	NP_599020.1:n.732+42A>C
NM_134259.1:c.732+42A>C	NP_599021.1:n.732+42A>C
XM_005262572.2:c.774+42A>C	XP_005262629.1:n.774+42A>C
XM_005262572.3:c.774+42A>C	XP_005262629.1:n.774+42A>C
XM_017030086.1:c.732+42A>C	XP_016885575.1:n.732+42A>C
XM_017030087.1:c.732+42A>C	XP_016885576.1:n.732+42A>C
XM_024452497.1:c.732+42A>C	XP_024308265.1:n.732+42A>C
NM_033284.2:c.732+42A>C MANE Select	NP_150600.1:n.732+42A>C
NM_134258.2:c.732+42A>C	NP_599020.1:n.732+42A>C
NM_134259.2:c.732+42A>C	NP_599021.1:n.732+42A>C