Canonical Allele Identifier: CA2241534748
Gene: CDH15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89179459C= , CM000678.2:g.89179459C= GRCh38
NC_000016.9:g.89245867C= , CM000678.1:g.89245867C= GRCh37
NC_000016.8:g.87773368C= NCBI36
NG_012055.1:g.12705C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000289746.3:c.86C= MANE Select ENSP00000289746.2:p.Thr29=
ENST00000289746.2:c.86C= ENSP00000289746.2:p.Thr29=
ENST00000521087.5:n.151C=
ENST00000524089.1:n.151C=
NM_004933.2:c.86C= NP_004924.1:p.Thr29=
XM_011522806.1:c.86C= XP_011521108.1:p.Thr29=
NM_004933.3:c.86C= MANE Select NP_004924.1:p.Thr29=