Canonical Allele Identifier: CA2241534907
Gene: CDH15 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89179619T= , CM000678.2:g.89179619T= GRCh38
NC_000016.9:g.89246027T= , CM000678.1:g.89246027T= GRCh37
NC_000016.8:g.87773528T= NCBI36
NG_012055.1:g.12865T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000289746.3:c.201+45T= MANE Select ENSP00000289746.2:n.201+45T=
ENST00000289746.2:c.201+45T= ENSP00000289746.2:n.201+45T=
ENST00000521087.5:n.266+45T=
ENST00000524089.1:n.266+45T=
NM_004933.2:c.201+45T= NP_004924.1:n.201+45T=
XM_011522806.1:c.201+45T= XP_011521108.1:n.201+45T=
NM_004933.3:c.201+45T= MANE Select NP_004924.1:n.201+45T=
Search 100 bp 5'
Search 100 bp 3'