Canonical Allele Identifier: CA284140157
Community Standard Title: NM_152342.4(CDYL2):c.1210G>T (p.Val404Phe)
Gene: CDYL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.80612634C>A , CM000678.2:g.80612634C>A GRCh38
NC_000016.9:g.80646531C>A , CM000678.1:g.80646531C>A GRCh37
NC_000016.8:g.79204032C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_152342.4:c.1210G>T MANE Select NP_689555.2:p.Val404Phe
ENST00000570137.7:c.1210G>T MANE Select ENSP00000476295.1:p.Val404Phe
NM_152342.2:c.1210G>T NP_689555.2:p.Val404Phe
NM_152342.3:c.1210G>T NP_689555.2:p.Val404Phe
ENST00000562812.5:c.1213G>T ENSP00000454546.1:p.Val405Phe
ENST00000563890.5:c.1213G>T ENSP00000455111.1:p.Val405Phe
ENST00000566173.3:c.1213G>T ENSP00000456934.1:p.Val405Phe
ENST00000570137.6:c.1210G>T ENSP00000476295.1:p.Val404Phe
XM_011522866.1:c.1312G>T XP_011521168.1:p.Val438Phe
XM_011522867.1:c.1201G>T XP_011521169.1:p.Val401Phe
XM_011522867.2:c.1201G>T XP_011521169.1:p.Val401Phe
XM_011522868.1:c.1033G>T XP_011521170.1:p.Val345Phe
XM_024450151.1:c.1033G>T XP_024305919.1:p.Val345Phe