Canonical Allele Identifier: CA2236588448

Gene: CDYL2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.80616732_80616733delinsTG , CM000678.2:g.80616732_80616733delinsTG	GRCh38
NC_000016.9:g.80650629_80650630delinsTG , CM000678.1:g.80650629_80650630delinsTG	GRCh37
NC_000016.8:g.79208130_79208131delinsTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000570137.7:c.1008-3897_1008-3896delinsCA MANE Select	ENSP00000476295.1:n.1008-3897_1008-3896delinsCA
ENST00000561616.2:n.459-3897_459-3896delinsCA
ENST00000562812.5:c.1011-3897_1011-3896delinsCA	ENSP00000454546.1:n.1011-3897_1011-3896delinsCA
ENST00000563890.5:c.1011-3897_1011-3896delinsCA	ENSP00000455111.1:n.1011-3897_1011-3896delinsCA
ENST00000566173.3:c.1011-3897_1011-3896delinsCA	ENSP00000456934.1:n.1011-3897_1011-3896delinsCA
ENST00000570137.6:c.1008-3897_1008-3896delinsCA	ENSP00000476295.1:n.1008-3897_1008-3896delinsCA
NM_152342.2:c.1008-3897_1008-3896delinsCA	NP_689555.2:n.1008-3897_1008-3896delinsCA
XM_011522866.1:c.1110-3897_1110-3896delinsCA	XP_011521168.1:n.1110-3897_1110-3896delinsCA
XM_011522867.1:c.999-3897_999-3896delinsCA	XP_011521169.1:n.999-3897_999-3896delinsCA
XM_011522868.1:c.831-3897_831-3896delinsCA	XP_011521170.1:n.831-3897_831-3896delinsCA
NM_152342.3:c.1008-3897_1008-3896delinsCA	NP_689555.2:n.1008-3897_1008-3896delinsCA
XM_011522867.2:c.999-3897_999-3896delinsCA	XP_011521169.1:n.999-3897_999-3896delinsCA
XM_024450151.1:c.831-3897_831-3896delinsCA	XP_024305919.1:n.831-3897_831-3896delinsCA
NM_152342.4:c.1008-3897_1008-3896delinsCA MANE Select	NP_689555.2:n.1008-3897_1008-3896delinsCA