Canonical Allele Identifier: CA2236588613

Gene: CDYL2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.80616839C= , CM000678.2:g.80616839C=	GRCh38
NC_000016.9:g.80650736C= , CM000678.1:g.80650736C=	GRCh37
NC_000016.8:g.79208237C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000570137.7:c.1007+3924G= MANE Select	ENSP00000476295.1:n.1007+3924G=
ENST00000561616.2:n.458+3924G=
ENST00000562812.5:c.1010+3924G=	ENSP00000454546.1:n.1010+3924G=
ENST00000563890.5:c.1010+3924G=	ENSP00000455111.1:n.1010+3924G=
ENST00000566173.3:c.1010+3924G=	ENSP00000456934.1:n.1010+3924G=
ENST00000570137.6:c.1007+3924G=	ENSP00000476295.1:n.1007+3924G=
NM_152342.2:c.1007+3924G=	NP_689555.2:n.1007+3924G=
XM_011522866.1:c.1109+3924G=	XP_011521168.1:n.1109+3924G=
XM_011522867.1:c.998+3924G=	XP_011521169.1:n.998+3924G=
XM_011522868.1:c.830+3924G=	XP_011521170.1:n.830+3924G=
NM_152342.3:c.1007+3924G=	NP_689555.2:n.1007+3924G=
XM_011522867.2:c.998+3924G=	XP_011521169.1:n.998+3924G=
XM_024450151.1:c.830+3924G=	XP_024305919.1:n.830+3924G=
NM_152342.4:c.1007+3924G= MANE Select	NP_689555.2:n.1007+3924G=