Canonical Allele Identifier: CA2236588444

Gene: CDYL2

Linked Data

• dbSNP Id: rs1370337527

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.80616727A>T , CM000678.2:g.80616727A>T	GRCh38
NC_000016.9:g.80650624A>T , CM000678.1:g.80650624A>T	GRCh37
NC_000016.8:g.79208125A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000570137.7:c.1008-3891T>A MANE Select	ENSP00000476295.1:n.1008-3891T>A
ENST00000561616.2:n.459-3891T>A
ENST00000562812.5:c.1011-3891T>A	ENSP00000454546.1:n.1011-3891T>A
ENST00000563890.5:c.1011-3891T>A	ENSP00000455111.1:n.1011-3891T>A
ENST00000566173.3:c.1011-3891T>A	ENSP00000456934.1:n.1011-3891T>A
ENST00000570137.6:c.1008-3891T>A	ENSP00000476295.1:n.1008-3891T>A
NM_152342.2:c.1008-3891T>A	NP_689555.2:n.1008-3891T>A
XM_011522866.1:c.1110-3891T>A	XP_011521168.1:n.1110-3891T>A
XM_011522867.1:c.999-3891T>A	XP_011521169.1:n.999-3891T>A
XM_011522868.1:c.831-3891T>A	XP_011521170.1:n.831-3891T>A
NM_152342.3:c.1008-3891T>A	NP_689555.2:n.1008-3891T>A
XM_011522867.2:c.999-3891T>A	XP_011521169.1:n.999-3891T>A
XM_024450151.1:c.831-3891T>A	XP_024305919.1:n.831-3891T>A
NM_152342.4:c.1008-3891T>A MANE Select	NP_689555.2:n.1008-3891T>A