Canonical Allele Identifier: CA2241534763
Gene: CDH15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89179482G= , CM000678.2:g.89179482G= GRCh38
NC_000016.9:g.89245890G= , CM000678.1:g.89245890G= GRCh37
NC_000016.8:g.87773391G= NCBI36
NG_012055.1:g.12728G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000289746.3:c.109G= MANE Select ENSP00000289746.2:p.Ala37=
ENST00000289746.2:c.109G= ENSP00000289746.2:p.Ala37=
ENST00000521087.5:n.174G=
ENST00000524089.1:n.174G=
NM_004933.2:c.109G= NP_004924.1:p.Ala37=
XM_011522806.1:c.109G= XP_011521108.1:p.Ala37=
NM_004933.3:c.109G= MANE Select NP_004924.1:p.Ala37=