Canonical Allele Identifier: CA14228731
Gene: CDYL2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs13329835

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.80616908A>G , CM000678.2:g.80616908A>G GRCh38
NC_000016.9:g.80650805A>G , CM000678.1:g.80650805A>G GRCh37
NC_000016.8:g.79208306A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_152342.2:c.1007+3855T>C VV NP_689555.2:p.=
XM_011522866.1:c.1109+3855T>C XP_011521168.1:p.=
XM_011522867.1:c.998+3855T>C XP_011521169.1:p.=
XM_011522868.1:c.830+3855T>C XP_011521170.1:p.=
NM_152342.3:c.1007+3855T>C VV NP_689555.2:p.=
XM_011522867.2:c.998+3855T>C XP_011521169.1:p.=
XM_024450151.1:c.830+3855T>C XP_024305919.1:p.=
NM_152342.4:c.1007+3855T>C VV MANE Preferred NP_689555.2:p.=
ENST00000561616.2:n.458+3855T>C
ENST00000562812.5:c.1010+3855T>C ENSP00000454546.1:p.=
ENST00000563890.5:c.1010+3855T>C ENSP00000455111.1:p.=
ENST00000566173.3:c.1010+3855T>C ENSP00000456934.1:p.=
ENST00000570137.6:c.1007+3855T>C ENSP00000476295.1:p.=