Canonical Allele Identifier: CA2241534927
Gene: CDH15 HGNC NCBI

Linked Data

dbSNP Id: rs772607179

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89179626T>G , CM000678.2:g.89179626T>G GRCh38
NC_000016.9:g.89246034T>G , CM000678.1:g.89246034T>G GRCh37
NC_000016.8:g.87773535T>G NCBI36
NG_012055.1:g.12872T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000289746.3:c.201+52T>G MANE Select ENSP00000289746.2:n.201+52T>G
ENST00000289746.2:c.201+52T>G ENSP00000289746.2:n.201+52T>G
ENST00000521087.5:n.266+52T>G
ENST00000524089.1:n.266+52T>G
NM_004933.2:c.201+52T>G NP_004924.1:n.201+52T>G
XM_011522806.1:c.201+52T>G XP_011521108.1:n.201+52T>G
NM_004933.3:c.201+52T>G MANE Select NP_004924.1:n.201+52T>G