Canonical Allele Identifier: CA2241534757
Gene: CDH15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89179473T= , CM000678.2:g.89179473T= GRCh38
NC_000016.9:g.89245881T= , CM000678.1:g.89245881T= GRCh37
NC_000016.8:g.87773382T= NCBI36
NG_012055.1:g.12719T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000289746.3:c.100T= MANE Select ENSP00000289746.2:p.Trp34=
ENST00000289746.2:c.100T= ENSP00000289746.2:p.Trp34=
ENST00000521087.5:n.165T=
ENST00000524089.1:n.165T=
NM_004933.2:c.100T= NP_004924.1:p.Trp34=
XM_011522806.1:c.100T= XP_011521108.1:p.Trp34=
NM_004933.3:c.100T= MANE Select NP_004924.1:p.Trp34=