Canonical Allele Identifier: CA2634929889
Gene: CDH15 HGNC NCBI

Linked Data

gnomAD v4: 16-89179606-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89179606A>T , CM000678.2:g.89179606A>T GRCh38
NC_000016.9:g.89246014A>T , CM000678.1:g.89246014A>T GRCh37
NC_000016.8:g.87773515A>T NCBI36
NG_012055.1:g.12852A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000289746.3:c.201+32A>T MANE Select ENSP00000289746.2:n.201+32A>T
ENST00000289746.2:c.201+32A>T ENSP00000289746.2:n.201+32A>T
ENST00000521087.5:n.266+32A>T
ENST00000524089.1:n.266+32A>T
NM_004933.2:c.201+32A>T NP_004924.1:n.201+32A>T
XM_011522806.1:c.201+32A>T XP_011521108.1:n.201+32A>T
NM_004933.3:c.201+32A>T MANE Select NP_004924.1:n.201+32A>T
Search 100 bp 5'
Search 100 bp 3'