Canonical Allele Identifier: CA2241534749
Gene: CDH15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89179460C= , CM000678.2:g.89179460C= GRCh38
NC_000016.9:g.89245868C= , CM000678.1:g.89245868C= GRCh37
NC_000016.8:g.87773369C= NCBI36
NG_012055.1:g.12706C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000289746.3:c.87C= MANE Select ENSP00000289746.2:p.Thr29=
ENST00000289746.2:c.87C= ENSP00000289746.2:p.Thr29=
ENST00000521087.5:n.152C=
ENST00000524089.1:n.152C=
NM_004933.2:c.87C= NP_004924.1:p.Thr29=
XM_011522806.1:c.87C= XP_011521108.1:p.Thr29=
NM_004933.3:c.87C= MANE Select NP_004924.1:p.Thr29=